Weight Bias

4

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

Condition / disease
Location
Status: Not yet recruiting

Fluid vs Weight 24 Hour Balance

Daily Fluid Balance vs Weight Change

Participants needed: 55
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Masarykova Nemocnice v Usti nad Labem, Krajska Zdravotni a.s.Updated: Mar 16, 2026
Eligibility criteria

age <18 years [+11]

Status: Not yet recruiting

Weight Bias Reducation Intervention With Nursing Students Using Simulation: The BRAVE Study

This randomized controlled trial will be a curriculum-embedded weight sensitivity training program. There will be two groups. The control group will receive the standard obesity lecture (SOL) and the intervention group will receive the BRAVE Intervention (BRAVE: Building Respect and Acceptance through Valuing Everybody); a Weight Bias Reduction (WBR) intervention. Both groups will have two simulation encounters with standardized patients who are living with obesity and the outcome will be to improve weight bias and increase weight sensitivity over one year. Participants will include second- and fourth-year nursing students. Two cohorts of nursing students will be recruited over two years during orientation for their NUR courses (n = 368); a combined total of 420 students are typically enrolled in these courses. Study participants will be randomized by 8-person simulation groups (clusters) to either the BRAVE intervention or SOL control group. They will then participate in the two simulation-based experiences and weight bias reduction education or standard obesity lecture, respectively, with a debriefing segment and educational components. To compare the efficacy of BRAVE groups to SOL groups in validated questionnaires will assess changing attitudes, beliefs, and clinical communication behaviors when comparing baseline to 3 months post-intervention, and one year after the intervention.

Participants needed: 368
Trial details
Age: 18-25Biological sex: AllType: InterventionalSponsor: Villanova UniversityUpdated: Jan 13, 2026Locations: 1
Eligibility criteria

Nursing students aged 18-25 [+1]

Non-nursing students [+3]

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: Recruiting

Addressing Weight Bias Internalization to Improve Adolescent Weight Management Outcomes: Randomized Pilot Trial

Weight stigma and weight bias internalization (WBI) are common among adolescents at higher weight statuses. WBI is associated with negative physical and mental health outcomes. The current study aims to test an intervention for weight stigma and WBI combined with an evidence-based adolescent weight management program. Eligible adolescents (13-17) will be assigned by chance to one of two groups: 1) a 4-week intervention focused on weight stigma and WBI followed by a 16-week behavioral weight management program; or 2) a 4-week health information control (to include non-weight-related health promotion topics such as smoking and skin cancer prevention) followed by the same 16-week weight management program but without the WBI and weight stigma content. Study outcomes will be assessed at the 4-week and post-treatment (20 week) timepoints.

Participants needed: 64
Trial details
Age: 13-17Biological sex: AllType: InterventionalSponsor: The Miriam HospitalUpdated: Sep 24, 2025Locations: 1
Eligibility criteria

Speak English; [+4]

Cognitive impairment or developmental delay impairing participation in a group s... [+3]