Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Eating Disorders from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 24
- Active, not recruiting: 3
- Completed: 16
- Other: 7
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00739362 — Effects of Brain Stimulation on Food Intake and Behavioral Weight Loss Treatment
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 148 |
| Study Type | INTERVENTIONAL |
| Conditions | Electric Stimulation Therapy; Obesity; Weight Loss; Eating |
| Interventions | ; |
This study will determine whether electrical stimulation of an area of the brain called the dorsolateral prefrontal cortex, which is important in determining the feeling of fullness after eating, affects how much food a person eats and weight loss over 4 weeks. It will also compare weight changes in people who attend weight loss counseling sessions and those who do not over this period of time….
NCT02390765 — Children s Growth and Behavior Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
| Enrollment | 1500 |
| Study Type | OBSERVATIONAL |
| Conditions | Obesity; Eating Behaviors; Healthy Volunteers |
Background:
- Studies show that many factors affect children’s eating behavior and health. These include sleep, mood, thinking skills, and genetics. Studying children over time may identify children at higher risk for eating-related health concerns.
Objective:
- To understand how genes and environment influence eating behavior and health over time.
Eligibility:
- Children ages 8-17 in g…
NCT04923087 — Impact of Auditory Stimulation in Eating Pleasure (EDERE 2021)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier Universitaire de Nice |
| Enrollment | 100 |
| Study Type | OBSERVATIONAL |
| Conditions | Frailty; Malnutrition; Anorexia; Presbycusis; Edentulism Nos |
| Interventions |
Background. Decreased taste and smell contribute to loss of appetite (anorexia), and the resulting protein-energy malnutrition increases the frailty of the elderly. The risk of falls, disability, infections and depression often requires them to be institutionalized. Elderly, undernourished and toothless patients often complain about the monotony of a soft, mixed-texture diet. In a previous stud…
NCT04697966 — Mechanisms and Predictors of Change in App-Based Mindfulness Training for Adolescents
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Mclean Hospital |
| Enrollment | 158 |
| Study Type | INTERVENTIONAL |
| Conditions | Rumination |
| Interventions | ; |
A growing body of research implicates rumination as being a transdiagnostic risk factor involved in the development of depression and anxiety in youth. Critically, mindfulness meditation has shown significant promise in targeting rumination, and ultimately improving depressive and anxiety symptoms. Mindfulness apps offer a convenient and cost-effective means for accessing mindfulness training, …
NCT05454046 — Food Intake Among Women and Men in Fertility Treatment
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Aalborg University Hospital |
| Enrollment | 4000 |
| Study Type | OBSERVATIONAL |
| Conditions | Infertility |
| Interventions |
Worldwide infertility is highly prevalent and lifestyle factors, such as food intake, could have an essential role in the success of a fertility treatment. The literature is not consistent and adequate for recommendations to the increasing number of women and men of reproductive age who ask for lifestyle guidance. Therefore, the aims of the Food & Fertility study will be to investigate the ass…
NCT05763849 — Interoceptive Exposure for Adolescents With Low Weight Eating Disorders
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Icahn School of Medicine at Mount Sinai |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Anorexia Nervosa |
| Interventions | ; |
This project includes a parallel group randomized controlled trial comparing two psychological treatments: 1) Exposure-based Family Therapy (IE) vs. 2) Family Based Therapy (FBT) for low weight eating disorders with 12 month follow-up. Primary outcomes are expected body weight and clinical impairment. Three mechanisms of change (Autonomous Eating, Non-Judgmental Body Awareness, and Extinction L…
NCT05858008 — Feasibility of Implementing Time-restricted Eating in Women With Mild Cognitive Impairment
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Julie Pendergast |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | Mild Cognitive Impairment |
| Interventions |
This study will investigate the feasibility of implementing a time-restricted eating intervention in females with mild cognitive impairment. Targeted therapeutic interventions that improve cognitive impairment and delay onset of ADRD are particularly important for females, who have twice the lifetime risk of developing AD, compared to males.
NCT06594913 — Eating Disorders Genetics Initiative 2
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of North Carolina, Chapel Hill |
| Enrollment | 20000 |
| Study Type | OBSERVATIONAL |
| Conditions | Anorexia Nervosa; Bulimia Nervosa; Binge-Eating Disorder; Avoidant Restrictive Food Intake Disorder |
| Interventions |
The overarching intention of the Eating Disorder Genetics Initiative 2 (EDGI2) is to increase sample size, diversity, and eating disorder phenotypes. The investigators are enrolling 20,000 new participants with anorexia nervosa (AN), bulimia nervosa (BN), binge-eating disorder (BED), avoidant/restrictive food intake disorder (ARFID), and controls in the US, Mexico, Australia, New Zealand, Swede…
NCT06491537 — Time-restricted Eating for Postpartum Weight Loss
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Postpartum Weight Retention; Overweight and Obesity |
| Interventions | ; |
This study is being done to assess the feasibility and acceptability of a time-restricted eating intervention among postpartum women with overweight/obesity.
NCT06118931 — Time-restricted Eating, Window Timing, Type 2 Diabetes Status and Sex on Glycemic Control
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Toronto |
| Enrollment | 123 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabetes Mellitus, Type 2; Obesity; Prediabetic State; Hyperglycemia |
| Interventions | ; ; |
This study will evaluate the effectiveness of time-restricted eating (TRE), which is a form of intermittent fasting. When performing TRE, individuals consume all of their calories within a specific time window and then only consume water or other no calorie drinks the rest of the day. TRE is performed each day. There is no restriction on the quality or amount of food that people can consume dur…
NCT07672821 — Time-Restricted Eating After Bariatric Surgery
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Medipol University |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity & Overweight; Bariatric Surgery; Weight Regain; Weight Regain Post Bariatric Surgery; Time Restricted Feeding |
| Interventions |
This study aims to compare the effects of time-restricted eating (TRE, 16/8) in adults with obesity who have and have not undergone bariatric surgery (BS). The study will include adults aged 18-65 years: those with obesity who have not undergone BS, and those who have experienced insufficient weight loss (IWL) or weight regain (WR) following BS. Both groups will follow a 16:8 time-restricted ea…
NCT06824974 — Time-restricted Eating and Healthy Eating in Patients With Metabolic Liver Disease or Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of California, San Diego |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Liver Cancer, Adult; MASH - Metabolic Dysfunction-Associated Steatohepatitis; Obesity and Overweight |
| Interventions |
This is a feasibility study that will collect data to assess the potential effect of nutritional intervention. This prospective single-site trial will enroll adult patients with liver diseases such as metabolic-dysfunction associated steatotic liver disease (MASLD), metabolic-dysfunction associated steatohepatitis (MASH), cirrhosis and/or hepatocellular carcinoma (HCC). Eligible individuals who…
NCT07135505 — Early Time-Restricted Eating in Older Adults With Hypertension
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension; Eating Behaviors |
| Interventions |
The purpose of this study is to find out how early time-restricted eating affects body rhythms and improves cardiometabolic health in older adults.
NCT07690176 — How the Body Processes Sugar After Eating, in People With Different Body Weights
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Wageningen University |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity & Overweight |
| Interventions | ; ; |
The goal of this clinical trial is to learn how a high-glycaemic meal affects the way the body processes glucose in healthy adults who are either lean or have obesity. The main questions it aims to answer are: Is the polyol pathway (conversion of glucose into sorbitol and fructose) more active after a hyperglycaemic meal? Is this pathway more active in individuals with obesity compared with lea…
NCT07202949 — A Clinical Trial of Extended (High) Treatment Dose Antibiotics in Combination With Methenamine Hippurate Compared to the Standard of Care (Either Prophylactic (Low) Dose Antibiotic Treatment or Methenamine Hippurate) in Females With Chronic Urinary Tract Infection
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | University College, London |
| Enrollment | 192 |
| Study Type | INTERVENTIONAL |
| Conditions | Chronic Urinary Tract Infection |
| Interventions | ; |
Chronic Urinary Tract Infection (UTI) is a type of UTI where symptoms are constant and occur every day, unlike recurrent UTIs, which come and go with symptom-free breaks in between. Current treatment for chronic UTI within the NHS is based on recommended guidelines for recurrent UTI. The standard approach typically includes one of the following treatments:
- Long-term, prophylactic (low) dose …
NCT07565129 — PrevED MR. Improving Emotion Dysregulation Through Mixed Reality Based Dialectical Behavioral Therapy in Adolescents and Young Adults at Risk of Developing Eating Disorders.
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Universitat Internacional de Catalunya |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | Eating Disorders; Emotion Dysregulation |
| Interventions |
The aim of this study is to evaluate the feasibility and preliminary effects of PrevED MR, a group-based preventive intervention for adolescents and young adults at risk of developing eating disorders. PrevED MR is based on dialectical behavior therapy skills and uses mixed reality and virtual reality activities to support emotion regulation, mindfulness, distress tolerance, and body-related ac…
NCT07542145 — MDMA Assisted Therapy for BN
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Icahn School of Medicine at Mount Sinai |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Bulimia Nervosa |
| Interventions | ; ; |
This project will evaluate MDMA Assisted Therapy (MDMA-AT) assisted psychotherapy for the treatment of Bulimia Nervosa (BN) over a 10-week period. Preliminary data suggests that MDMA can facilitate heightened openness and reduce anxiety. This study will determine whether MDMA-assisted therapy can serve as a new treatment for BN. Participants are assigned to one of three groups: MDMA-AT, MDMA-AT…
NCT07387796 — Clinical and Neurobehavioral Changes With Weight Loss Drug Discontinuation and Reinitiation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | The University of Texas at Dallas |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Drug Discontinuation; Substance Use Disorders; Eating Behavior Changes; Tirzepatide |
| Interventions |
The goal of this clinical study with research procedures is to learn how stopping and restarting tirzepatide (a medication that helps regulate blood sugar and appetite) affects brain activity, behavior, and health in adults ages 18-70 who are currently taking tirzepatide. Specifically, the study aims to examine how a short pause in tirzepatide affects hunger, mood, sleep, and daily functioning;…
NCT07591428 — Reset Challenge: Reducing High-risk Drinking for Cancer Prevention
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Oklahoma |
| Enrollment | 150 |
| Study Type | INTERVENTIONAL |
| Conditions | Alcohol Drinking; Heavy Drinking; Binge Drinking |
| Interventions |
This is a single-arm, non-randomized, prospective study to evaluate the feasibility and preliminary efficacy of a 30-day mobile Health (mHealth) Reset Challenge for reducing high-risk drinking.
NCT07378072 — Efficacy of 12-week Daytime Restricted Eating on Hepatic Steatosis of Obesity
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Nantes University Hospital |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | MASLD (Metabolic Dysfunction-Associated Steatotic Liver Disease) |
| Interventions | ; |
The objective of this study is to demonstrate that an < or equal to 8-hour time-restricted eating (i.e., fasting for at least 16 hours every day), not focusing on reducing caloric intake, reduces intra-hepatic fat in patients with obesity and Metabolic dysfunction-Associated Steatotic liver Disease (MASLD).
NCT07600671 — Eating Disorder Dynamic Intervention
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Trustees of Dartmouth College |
| Enrollment | 170 |
| Study Type | INTERVENTIONAL |
| Conditions | Eating Disorders; Anorexia Nervosa; Bulimia Nervosa; Binge Eating Disorder; Other Specified Feeding or Eating Disorder |
| Interventions |
The goal of this study is to develop and test a digital program to help people with eating disorders in their everyday lives. The program uses brief surveys and sensor data collected by smartphones to understand when someone may be at higher risk for behaviors like restricting food, binge eating, or using unhealthy weight control behaviors.
NCT07685483 — Dramatherapy for Psychological and Social Well-Being in Obesity and Bariatric Care
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Universite du Littoral Cote d’Opale |
| Enrollment | 250 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity (Disorder); Obesity & Overweight; Eating Disorders; Bariatric Surgery |
| Interventions | ; |
Obesity is currently a major public health challenge in France, particularly in the Hauts-de-France region, where prevalence exceeds 20% of the adult population. Bariatric surgery has considerably increased over the last two decades and is now recognized as an effective therapeutic option within a multidisciplinary care pathway. However, many patients continue to experience difficulties related…
NCT07318207 — Time-restricted Eating for Patients With Type 2 Diabetes
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Justin (Matt) Thomas |
| Enrollment | 102 |
| Study Type | INTERVENTIONAL |
| Conditions | Type 2 Diabetes |
| Interventions |
This is a single-arm pragmatic clinical trial of time-restricted eating in patients with type 2 diabetes. Patients will be recruited from the University of Kentucky Barnstable Brown Diabetes Center. Subjects will participate in a 10-hour time-restricted eating intervention for 1-year.
NCT06802172 — Effect of Meal Timing During Cancer Treatment in Patients in Alaska: A Randomized Clinical Trial
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fred Hutchinson Cancer Center |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Rectal Cancer Stage II; Rectal Cancer Stage III; Breast Cancer Stage I; Rectal Cancer Stage IV; Breast Cancer Stage II |
| Interventions | ; ; |
The goal of this clinical trial is to test meal-timing as a novel and sustainable interventional approach during cancer treatment to improve therapeutic response and metabolic health in an understudied population. This clinical trial will enroll patients with rectal or breast cancer receiving neoadjuvant treatment at the Alaska Native Medical Center (ANMC), which is part of the Alaska Native Tr…
Active, Not Recruiting
NCT04057716 — Project REST: Regulation of Eating and Sleep Topography
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Pittsburgh |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity, Childhood; Binge Eating; Sleep; Self-regulation |
| Interventions | ; |
Overweight/obesity and inadequate sleep are prevalent, and frequently co-occurring, health risks among children, both of which are associated with serious medical and psychosocial health complications including risk for cardiovascular disease. Although the investigator’s data suggest that disrupted or shortened sleep may be causally associated with increased energy intake and weight gain in chi…
NCT04213014 — Guys/Girls Opt for Activities for Life Trial (GOAL) to Increase Young Adolescents’ Physical Activity and Healthy Eating
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Michigan State University |
| Enrollment | 935 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity, Adolescent |
| Interventions |
In this 2-phase trial (R61/R33), we propose Guys/Girls Opt for Activities for Life (GOAL). Guided by Self-Determination Theory and the Information-Motivation-Behavioral Skills Model, GOAL will target the school and home environment to increase young adolescents’ physical activity (PA) and healthy eating by increasing important factors at the individual-level: motivation and self-efficacy; and s…
NCT06819813 — Project VIBE: Virtual Intervention for Binge Eating in Adolescents
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Pittsburgh |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity; Binge-Eating Disorder; Binge Eating |
| Interventions |
The aim of this project is to pilot test a novel mobile app intervention for adolescents with dysregulated eating behaviors and elevated weight status. This intervention will incorporate evidence-informed strategies targeting self-regulation into cognitive-behavioral treatment for maladaptive eating. Adolescents will use the app for 16 weeks and provide feedback on its usability and effectivene…
Not Yet Recruiting
NCT07021937 — Brain Plasticity and GLP-1 Receptor Agonist Treatment for Obesity
| Status | Not yet recruiting |
| Phase | Phase 3 |
| Sponsor | University of Colorado, Denver |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Obesity/Therapy |
| Interventions | ; |
Glucagon-like peptide 1 receptor agonists (GLP-1RA), such as Ozempic and Wegovy, have been rapidly adopted for the treatment of obesity in both youth and adults. However, despite this rapid adoption and the known GLP-1RA mechanism of action for weight loss, which targets brain circuits responsible for appetite and eating behaviors, almost nothing is known about how these drugs affect the brain …
NCT07678554 — Overvaluation of Weight and Shape Intervention vs The Body Project
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Stanford University |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Body Image; Mental Health Outcomes; Eating Disorders; Body Dysmorphic Disorders; Self-esteem |
| Interventions | ; |
Priorities aims to reduce body image concerns, prevent eating disorders, bolster self-esteem, and promote mental and emotional health by helping participants identify and nurture alternative sources of self-worth. Priorities would use group discussions, role-plays & behavioral challenges, homework assignments & letter-writing, and self-worth activism to achieve this. The Priorities interventi…
NCT06690294 — Assessing the Impact of Perceptions of Unpredictability on Objective Measures of Food Consumption and Metabolism
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
| Enrollment | 110 |
| Study Type | OBSERVATIONAL |
| Conditions | Healthy Volunteer; Obestity |
Background:
Many people in the United States are overweight or obese. This natural history study will look into how life events during childhood can impact eating behaviors and weight gain as adults.
Objective:
To explore how childhood experiences affect adult eating behaviors.
Eligibility:
Healthy people aged 18 to 60 years.
Design:
Participants will have 3 clinic visits.
They will be …
NCT07661823 — QAIAx (AIhealth4U) - AI Public Health Central: Microcity-A (re Quantum AI Agency Aka AI City Hall Project, UPSTO App Nos. 64/074,526, 64/063,557, 63/903,181, 63/729,428
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Veterans Recovery Network Inc. |
| Enrollment | 1000000 |
| Study Type | INTERVENTIONAL |
| Conditions | Asperger’s Disorder; Asperger Disorder; Autism Disorder; Autism; ADHD - Attention Deficit Disorder With Hyperactivity |
| Interventions | ; |
BRIEF SUMMARY
A. “What is the purpose of this study?”
This study will test whether the “AI City Hall Project” (QAIAx), a quantum artificial intelligence (AI) public health agency, can provide free or low-cost behavioral and mental health services inside self-contained, dome-enclosed communities called “Microcities”. Researchers want to see if AI-managed public administration, AI humanoid robo…
NCT07690033 — Eating Behavior and ADHD
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Sohag University |
| Enrollment | 150 |
| Study Type | OBSERVATIONAL |
| Conditions | Eating Behavior and Snack Consumption |
| Interventions |
The goal of this observational study is to learn about the effect of eating behavior and snack consumption patterns among children with ADHD. The main question it aims to answer is:
Does snack consumption increase insidenc and severity of ADHD?? Participants will answer survey questions about their eating behavior and snack consumption patterns.
NCT07503093 — Pilot Study of Sensor-Informed Smartphone-based Mental Health Interventions for Mood in Early Psychosis
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Mclean Hospital |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Psychosis; Anxiety; Depression; Rumination |
| Interventions | ; ; |
The aim of this trial is to evaluate the feasibility and preliminary efficacy of using passive smartphone sensors to detect moments of heightened negative mood and inform the timing of brief mental health interventions, such as mindfulness exercises and psychoeducation, in adults with early psychosis.
Enrolling by Invitation
NCT07623889 — Rumination-Tailored Guided Internet-Based CBT-I for University Students
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Shahid Beheshti University of Medical Sciences |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Insomnia; Insomnia Disorder |
| Interventions | ; |
The goal of this clinical trial is to evaluate whether adding rumination-tailored, rule-based personalized feedback to guided internet-based cognitive behavioral therapy for insomnia (iCBT-I) improves treatment outcomes in university students with insomnia symptoms.
The main questions it aims to answer are:
Does rumination-tailored feedback improve insomnia severity compared to standard guide…
Completed Trials
NCT04127214 — The ITA Model of Integrated Treatment of Eating Disorders
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Barcelona |
| Enrollment | 800 |
| Study Type | OBSERVATIONAL |
| Conditions | Eating Disorders; Anorexia Nervosa; Bulimia Nervosa; Binge Eating; Eating Disorders in Adolescence |
| Interventions |
This is a naturalistic study implementing a routine assessment to monitor the evolution of the patients with eating disorders being treated in various centers of “ITA salud mental” in Spain.
NCT04360018 — Effect of Acute Alcohol Intoxication on Neural Processes During Decisions to Engage in HIV Risk Behaviors
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | National Institute on Alcohol Abuse and Alcoholism (NIAAA) |
| Enrollment | 20 |
| Study Type | INTERVENTIONAL |
| Conditions | Alcohol Consumption |
| Interventions | ; |
Background:
People who binge drink are more likely to have risky sexual encounters, and alcohol changes brain activity associated with reward decisions related to those behaviors. Researchers want to better understand how alcohol s effects on risky sexual behavior that might lead people to contract sexually transmitted diseases (STDs) like HIV, the virus that causes AIDS.
Objective:
To study…
NCT07670910 — University of Georgia Mind Your Heart Pilot Study
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Georgia |
| Enrollment | 37 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension (HTN); Obesity & Overweight |
| Interventions | ; |
The goal of this observational study is to learn if nutrition education can improve eating habits and health outcomes in adults. The main questions it aims to answer are:
- Does participation in a 6-week nutrition education program improve dietary behaviors?
- Does participation in the program improve health measures such as blood lipids, blood pressure, and eye nutrient levels?
Participant…
NCT05732935 — Fasting ENHANCE Pilot Study
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Florida |
| Enrollment | 45 |
| Study Type | INTERVENTIONAL |
| Conditions | Overweight and Obesity; Time Restricted Feeding; Alzheimer Disease |
| Interventions | ; |
Grounded in the principles of geroscience, the proposed Fasting ENHANCE study will test whether a time restricted eating (TRE) regimen can improve cognitive function and other aspects of successful aging in a safe and sustainable manner in at risk overweight older adults. Specifically, this study will evaluate whether TRE can improve cognitive and physical function, as well as self-reported sle…
NCT05997316 — Time Restricted Eating for Metabolic and Psychological Optimization
| Status | Completed |
| Phase | N/A |
| Sponsor | University of North Carolina, Chapel Hill |
| Enrollment | 33 |
| Study Type | INTERVENTIONAL |
| Conditions | Mild Cognitive Impairment; Obesity |
| Interventions |
Obesity and related metabolic comorbidities have been associated with more than a 4-fold increased risk of incident cognitive impairment, including Alzheimer’s disease and related dementias (ADRD). Dysfunctional metabolic flexibility is increasingly recognized as a critical mechanism linking metabolic risk factors to risk of cognitive impairment, although few studies portable behavioral strateg…
NCT07663916 — Dog-Assisted Therapy in Adolescents Attending a Child and Adolescent Mental Health Day Hospital
| Status | Completed |
| Phase | N/A |
| Sponsor | Hospital Clinic of Barcelona |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Mental Health Disorders in Adolescents; Emotional Dysregulation; Anxiety Disorders; Depressive Disorders; Eating Disorders |
| Interventions | ; |
This study aimed to evaluate the feasibility and effectiveness of a dog-assisted therapy program integrated into a Child and Adolescent Mental Health Day Hospital, as well as to explore participants’ subjective experiences.
Mental health disorders in adolescence are common and often require intensive treatment approaches. Day hospitals provide structured care while allowing adolescents to rema…
NCT05954728 — Cognitive-behavioral Therapy vs. Nutrition Counseling for Avoidant/Restrictive Food Intake Disorder
| Status | Completed |
| Phase | N/A |
| Sponsor | Massachusetts General Hospital |
| Enrollment | 53 |
| Study Type | INTERVENTIONAL |
| Conditions | Avoidant/Restrictive Food Intake Disorder (ARFID) |
| Interventions | ; |
This study is a randomized controlledlinical trial, assessing the efficacy of cognitive- behavioral therapy (CBT-AR) and nutrition counseling for avoidant/restrictive food intake disorder (ARFID) for children and adolescents (ages 10-18 years).
NCT06345040 — The Dialogue Study: A Virtual-reality Based Treatment for Eating Disorders
| Status | Completed |
| Phase | N/A |
| Sponsor | University Hospital Bispebjerg and Frederiksberg |
| Enrollment | 96 |
| Study Type | INTERVENTIONAL |
| Conditions | Eating Disorders; Anorexia Nervosa; Bulimia Nervosa |
| Interventions | ; |
The Dialogue Study is a randomized, assessor-blinded parallel-groups superiority clinical trial fulfilling the CONSORT criteria for non-pharmacological treatment. The aim of the trial is to investigate the effect of a new virtual reality based psychotherapy for eating disorders. A total of 96 participants with a diagnosis of anorexia nervosa or bulimia nervosa will be allocated to either Virtua…
NCT06349460 — Trial to Optimize Just-in-Time Adaptive Intervention for Binge Eating & Weight-related Behaviors
| Status | Completed |
| Phase | N/A |
| Sponsor | Northwestern University |
| Enrollment | 300 |
| Study Type | INTERVENTIONAL |
| Conditions | Binge Eating; Obesity |
| Interventions |
The purpose of this study is to conduct a micro-randomized trial to learn which evidence-based targets within a mobile intervention for binge eating and weight-related behaviors are most impactful for which people and in what sequence.
NCT05609409 — FlexED: A Digital, Gamified Early Intervention for Eating Disorders
| Status | Completed |
| Phase | N/A |
| Sponsor | Duke University |
| Enrollment | 34 |
| Study Type | INTERVENTIONAL |
| Conditions | Eating Disorders; Body Image |
| Interventions |
The goal of this clinical trial is to test a new intervention for body-image distress to reduce eating disorder symptoms in young women and girls between the ages of 15-25 years old.
Participants complete up to 8 digital sessions using their mobile phone that include a character, story line and interactive exercises, games and digital rewards. Everyone in the study completes the intervention a…
NCT06463470 — Cognitive Behavioural Therapy for Avoidant/Restrictive Food Intake Disorder (CBT-AR)
| Status | Completed |
| Phase | N/A |
| Sponsor | Orygen |
| Enrollment | 3 |
| Study Type | INTERVENTIONAL |
| Conditions | Avoidant/Restrictive Food Intake Disorder (ARFID) |
| Interventions |
CBT-AR describes an adaption of cognitive behavioural therapy for use with individuals diagnosed with Avoidant/Restrictive Food Intake Disorder (ARFID). The purpose of this evaluation is to determine the feasibility, acceptability and effectiveness of this treatment.
It is hypothesised that this treatment will be feasible and acceptable to clinicians, carers and patients and will be effective …
NCT06624150 — tDCS and Cognitive Training for Restrictive Eating Disorders
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | University of Minnesota |
| Enrollment | 1 |
| Study Type | INTERVENTIONAL |
| Conditions | Anorexia Nervosa; Atypical Anorexia Nervosa |
| Interventions | ; |
This study looks at adults with restrictive eating disorders who are currently receiving outpatient treatment for their eating disorder to examine whether a new brain stimulation technique called non-invasive transcranial direct current stimulation (tDCS) can enhance brain training. Participation involves interviews, assessments, 10 sessions of brain stimulation (active or sham), and computeriz…
NCT07677020 — Anorexia Prevention in Female College Students
| Status | Completed |
| Phase | N/A |
| Sponsor | Jinan University Guangzhou |
| Enrollment | 135 |
| Study Type | INTERVENTIONAL |
| Conditions | Eating Disorder Risk; Body Shape Concern |
| Interventions | ; ; |
This study evaluated whether an acceptance-based embodied movement program can reduce eating disorder risk and body shape concerns in female college students at elevated risk. A total of 135 female undergraduate and graduate students were randomly assigned to one of three groups: acceptance-based embodied movement, functional fitness control, or psychoeducation. The intervention lasted 8 weeks,…
NCT07079046 — Efficacy of Satisens® in Reducing Emotional Eating
| Status | Completed |
| Phase | N/A |
| Sponsor | José Enrique de la Rubia Ortí, Ph |
| Enrollment | 84 |
| Study Type | INTERVENTIONAL |
| Conditions | Emotional Eating; Overweight or Obesity; Hormonal Changes; Neurotransmitter Agents; Food Cravings |
| Interventions | ; |
This study evaluates the efficacy of Satisens®, a dietary supplement composed of plant extracts, in reducing emotional eating and sweet cravings in healthy adults. The study will analyze hormonal, neurotransmitter, and inflammatory markers to understand the underlying mechanisms.
NCT07238816 — A Research Study Looking at How Food Intake Affects Inno8 in the Body of Healthy People
| Status | Completed |
| Phase | Phase 1 |
| Sponsor | Novo Nordisk A/S |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Haemophilia A |
| Interventions |
The purpose of this study is to test a new medicine called Inno8. The study will test how eating and drinking before and after taking Inno8 affects how well it is absorbed in the stomach. The study consists of four arms. Participants will take the study medicine after an overnight fast. How long participants will need to fast depends on which group participants are in. After taking the study me…
NCT07671443 — Early Time-Restricted Eating in Young Judo Athletes
| Status | Completed |
| Phase | N/A |
| Sponsor | University of Manouba |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Nutrition, Healthy; Muscle Damage; Time Restricted Eating; Anxiety; Self Confidence |
| Interventions |
This study investigates the effects of a 5-month early time-restricted eating (e-TRE) intervention on body composition, muscle damage biomarkers, and psychological variables in highly trained young male judo athletes. One hundred participants were randomly assigned to either an e-TRE group or a control group. The e-TRE group followed a 16:8 fasting protocol (07:00-15:00 eating window) while mai…