Body Image Disturbance

7

Review clinical trials related to Body Image Disturbance. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Relationships Between Nomophobia Levels and Perceived Stress, Body Image and Food Addiction Among University Students

The purpose of this study is to examine the effects of nomophobia levels on stress, food addiction, and body image among undergraduate students aged 18-30 at Bahçeşehir University, Faculty of Health Sciences. The primary questions it aims to answer are: * Is there a statistically significant relationship between nomophobia levels and perceived stress, food addiction, and body image among university students? * Is there a correlation between objective anthropometric data (body fat percentage, skeletal muscle mass) measured via Bioelectrical Impedance Analysis (BIA), waist/hip circumference measurements, and the individual's perceived body image?

Participants needed: 150
Trial details
Age: 18-30Biological sex: AllType: ObservationalSponsor: Bahçeşehir UniversityUpdated: Apr 17, 2026Locations: 1
Eligibility criteria

Being an active smartphone user [+3]

Individuals with a current diagnosis of an eating disorder (e.g., anorexia nervo... [+5]

Status: Recruiting

Lifestyle Intervention for Obesity and Eating Disorder Prevention in Transgender Adolescents

Transgender and gender-diverse adolescents are at increased risk for obesity, disordered eating behaviors, body dissatisfaction, and reduced quality of life due to minority stress and structural inequities. However, no structured lifestyle interventions specifically tailored to this population have been developed. This randomized controlled trial aims to evaluate the effectiveness of a 6-month interdisciplinary lifestyle intervention designed to prevent obesity and eating disorders in transgender and gender-diverse adolescents aged 10-14 years. Participants will be randomized (1:1) to either an intervention group receiving monthly group sessions (for adolescents and caregivers separately) and weekly supportive messages, or a control group receiving standard outpatient care and general health recommendations. The primary outcome is quality of life measured by the WHOQOL-BREF. Secondary outcomes include eating disorder symptoms, body image, diet quality, physical activity levels, sedentary behavior, body composition, and anthropometric measures.

Participants needed: 24
Trial details
Age: 10-14Biological sex: AllType: InterventionalSponsor: University of Sao PauloUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

Aged 10-14 years [+1]

Current diagnosis of eating disorder requiring specialized treatment [+2]

Status: Recruiting

Acceptability and Feasibility of a Single-Session Online Parent-Focused Intervention Targeting Child Body Image Development

Body image concerns have been linked to diverse mental health issues, including depression and disordered eating. Disordered eating can develop into clinically significant eating disorders, which are associated with serious negative impacts on psychological and physical well-being, and can adversely impact developmental trajectories in children and adolescents. Given limitations in the eating disorder intervention literature, it is important to invest in effective eating disorder prevention programs. Evidence suggests that children can recognize the existence of societal appearance ideals as early as age 3; thus, this study examines the acceptability and feasibility of a single-session, online, parent-focused intervention targeting predictors of body image disturbance in young children.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University at AlbanyUpdated: Dec 18, 2025Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Testing SHAPE: A Single-Session Intervention Targeting Binge Eating in Women Through Assessment and Values-Based Strategies

The goal of this controlled trial is to learn whether a brief single-session intervention (SSI) can reduce binge eating symptoms by targeting overvaluation of weight/shape in women with recurrent binge eating. The main questions it aims to answer are: * Does assessment alone reduce binge eating severity and overvaluation of weight/shape compared to a control group undergoing minimal assessment? * Does adding a values-based reflection and goal-setting component (the full SHAPE intervention) add benefits beyond the assessment alone? Researchers will compare three groups: 1. assessment-only, 2. full SHAPE intervention, and 3. minimal assessment control to see if both active conditions outperform the control, and whether the full intervention adds any benefits beyond the assessment itself Participants will: * Complete a semi-structured eating disorder assessment (Eating Disorder Examination) * Depending on assignment, also complete a values-based reflection and goal-setting exercise with psychoeducation * Complete follow-up assessments evaluating binge eating severity, overvaluation of weight/shape, clinical impairment, binge frequency, and related outcomes.

Participants needed: 56
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Taylor RezeppaUpdated: Oct 20, 2025Locations: 1
Eligibility criteria

≥ 18 years old [+4]

< 18 years old [+5]

Status: Recruiting

Interoceptive Mechanisms of Body Image Disturbance in Anorexia Nervosa

The proposed study utilizes a randomized experimental therapeutics design to test a mechanistic framework linking interoceptive processing and disturbed body image, with the purpose of informing the development of future therapies for body image dissatisfaction in anorexia nervosa (AN). A sample of 102 participants will be recruited from the Laureate Eating Disorder Program (LEDP). After being randomized, participants will all receive a one-hour session of acceptance- and mindfulness-based training with a therapist (the introduction session). They will then receive either the interoceptively focused treatment (IFT) or exteroceptively focused treatment (EFT) condition based on randomization. In the IFT condition participants will engage in floatation-REST (Reduced Environmental Stimulation Therapy) while practicing acceptance and mindfulness-based principles. The EFT condition is an exteroceptive intervention in which participants will be asked to view pre-recorded videos of acceptance and mindfulness-based skills to aid in the practice of these skills. Each condition will consist of one introduction session and three experimental sessions. All participants will then return for follow-up measures. Assessed outcomes will include acute changes in body image disturbance (BID) and interoception. Further, longitudinal intervention effects on self-reported eating disorder symptoms, body image dissatisfaction, and interoception; behavioral measures of interoception and body image dissatisfaction; and resting state and interoceptive functioning during functional magnetic resonance imaging (fMRI) will be explored.

Participants needed: 102
Trial details
Age: 13-50Biological sex: FemaleType: InterventionalSponsor: Laureate Institute for Brain Research, Inc.Updated: Sep 26, 2025Locations: 1
Eligibility criteria

Primary diagnosis of anorexia nervosa [+13]

Active suicidal ideation with plan and intent [+9]

Status: Recruiting

Building a Renewed ImaGe After Head & Neck Cancer Treatment (BRIGHT) Multi-Site RCT

In this multi-center randomized clinical trial, head and neck cancer (HNC) survivors with clinically significant body image distress (BID) (N=180) will be randomized to BRIGHT (a brief video tele-cognitive behavioral therapy intervention) or Attention Control (AC, a manualized tele-supportive care intervention that controls for professional attention, dose, delivery method, and common factors). HNC survivors will complete IMAGE-HN (a validated patient-reported outcome measure \[PROM\] of HNC-related body image distress \[BID\]; primary endpoint), measures of psychological and social well-being and quality of life (QOL), and measures of theory-derived mechanisms of change underlying BRIGHT (mediators).

Participants needed: 180
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Medical University of South CarolinaUpdated: Sep 24, 2025Locations: 5
Eligibility criteria

Age > 18 years on the day of informed consent [+9]

Inability to speak or read English [+2]

Status: Recruiting

Adolescent Chatbot

The purpose of this study is to test an eating disorders prevention digital chatbot program in a diverse group of adolescents.

Participants needed: 400
Trial details
Phase: Phase 2Age: 13-17Biological sex: AllType: InterventionalSponsor: Washington University School of MedicineUpdated: Jul 31, 2025Locations: 1
Eligibility criteria

13 - 17 years old [+5]

Below 13 or older than 17 years of age [+6]