Skip to content

Lifestyle Intervention for Obesity and Eating Disorder Prevention in Transgender Adolescents

Lifestyle Intervention to Prevent Obesity and Eating Disorders in Transgender and Gender-Diverse Adolescents: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07466069
Enrollment
24
Registered
2026-03-12
Start date
2026-03-01
Completion date
2026-12-01
Last updated
2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Body Image Disturbance, Eating Disorders, Gender Diverse Populations, Obesity & Overweight

Keywords

Transgender, Adolescent, Gender-diverse, Lifestyle, Eating disorders, Obesity

Brief summary

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.

Detailed description

This study is a parallel-group randomized controlled trial conducted at the Lifestyle Medicine Center, Faculty of Medicine, University of São Paulo (FMUSP), Brazil. Participants will be recruited from the Gender Identity and Sexual Orientation Outpatient Clinic (AMTIGOS) at the Institute of Psychiatry, Hospital das Clínicas, University of São Paulo. Eligible transgender and gender-diverse adolescents aged 10 to 14 years receiving care at AMTIGOS will be invited to participate. After baseline assessments, participants will be randomly assigned (1:1), in blocks of six, to either: 1. an interdisciplinary lifestyle intervention plus usual outpatient care; or 2. usual outpatient care plus a single session of general health recommendations. The 6-month intervention is grounded in Social Cognitive Theory and incorporates gender-affirmative principles and an intersectional framework. The intervention includes: * Monthly group sessions for adolescents * Monthly educational group sessions for caregivers * Weekly reinforcement messages The program focuses on promoting healthy eating behaviors, increasing physical activity, reducing sedentary behavior, preventing unhealthy weight-control practices, and fostering positive body image and body appreciation. The control group will receive standard outpatient follow-up at AMTIGOS and a single individual session including general recommendations regarding healthy eating, physical activity, body acceptance, and avoidance of unhealthy weight-control behaviors. Outcomes will be assessed at baseline and after 6 months. The primary outcome is quality of life measured by the WHOQOL-BREF. Secondary outcomes include eating disorder symptoms, body image, dietary quality, physical activity, sedentary behavior, body composition, and anthropometric measures.

Interventions

BEHAVIORALTransForm Health Program

A 6-month structured intervention including monthly adolescent group sessions, monthly caregiver sessions, monthly individual goal-setting meetings, and weekly reinforcement messages focused on healthy eating, physical activity, body appreciation, and prevention of unhealthy weight-control behaviors.

Sponsors

University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

Assessors of post-intervention body composition (DEXA) will be blinded to participants' group allocation.

Intervention model description

Experimental group and no intervention group (usual care group)

Eligibility

Sex/Gender
ALL
Age
10 Years to 14 Years
Healthy volunteers
No

Inclusion criteria

* Aged 10-14 years * Self-identified as transgender or gender-diverse

Exclusion criteria

* Current diagnosis of eating disorder requiring specialized treatment * Severe psychiatric instability * Cognitive impairment limiting participation

Design outcomes

Primary

MeasureTime frameDescription
Quality of Life (World Health Organization Quality of Life - BREF)Baseline and 6 monthsQuality of life will be measured using the World Health Organization Quality of Life - BREF (WHOQOL-BREF) questionnaire. The WHOQOL-BREF consists of 26 items covering four domains (physical health, psychological health, social relationships, and environment). Domain scores are transformed to a scale ranging from 0 to 100, with higher scores indicating better quality of life.

Secondary

MeasureTime frameDescription
Body fatBaseline and 6 monthsBody fat will be measured by dual-energy X-ray absorptiometry (DEXA).
Muscle massBaseline and 6 monthsMuscle mass will be measured by dual-energy X-ray absorptiometry (DEXA).
Bone densityBaseline and 6 monthsBone density will be measured by dual-energy X-ray absorptiometry (DEXA).
Body mass index (BMI)Baseline and 6 monthsBMI Z-score will be assessed by weight (kg) and height (m) that will be combined to report BMI in kg/m\^2 Z-score according to the World Health Organization growth curves.
Food consumptionBaseline and 6 monthsFood consumption will be assessed by three 24h food records.
Food insecurityBaseline and 6 monthsFood insecurity will be assessed using the Brazilian Food Insecurity Scale (EBIA), a 14-item questionnaire assessing household access to food in the previous 90 days. The total score ranges from 0 to 14, with higher scores indicating greater food insecurity.
Diet quality (Diet Quality Scale - ESQUADA)Baseline and 6 monthsDiet quality will be assessed using the Diet Quality Scale (ESQUADA - Escala de Qualidade da Dieta), a questionnaire based on the Brazilian Dietary Guidelines. The total score ranges from 0 to 100, with higher scores indicating better diet quality.
Diet quality (Health Eating Index-2020)Baseline and 6 monthsDiet quality will also be assessed using the Healthy Eating Index-2020 (HEI-2020), a measure of adherence to the Dietary Guidelines for Americans. The total score ranges from 0 to 100, with higher scores indicating better diet quality.
Food choice motivesBaseline and 6 monthsDeterminants of food choice will be assessed using the Eating Motivation Survey - Brief Version (TEMS), a questionnaire assessing motivations underlying food choices across multiple domains. Items are rated on a 5-point Likert scale ranging from 1 to 5, with higher scores indicating stronger endorsement of the respective eating motivation.
Screening for eating disordersBaseline and 6 monthsScreening for eating disorders will be conducted using the SCOFF questionnaire, a 5-item screening tool with yes/no responses. Scores range from 0 to 5, with higher scores indicating greater likelihood of an eating disorder. A score of 2 or more positive responses suggests a possible eating disorder and indicates the need for further assessment.
Eating disorders symptomsBaseline and 6 monthsEating disorder symptoms will be assessed using the Eating Disorder Examination Questionnaire (EDE-Q), a 28-item self-report instrument assessing eating disorder psychopathology over the previous 28 days. Items are rated on a 7-point scale ranging from 0 to 6, with higher scores indicating greater eating disorder psychopathology. The global score ranges from 0 to 6, representing the mean of four subscale scores
Body image dissatisfactionBaseline and 6 months.Body dissatisfaction will be assessed using the Body Shape Questionnaire (BSQ), a 34-item questionnaire measuring concerns about body shape. Items are rated on a 6-point Likert scale, with total scores ranging from 34 to 204, where higher scores indicate greater body dissatisfaction.
Body image appreciationBaseline and 6 months.Body image apprciation will be assessed using the Body Appreciation Scale-2 (BAS-2), a 10-item questionnaire evaluating body appreciation and respect for one's body. Items are rated on a 5-point Likert scale, with total scores ranging from 10 to 50, where higher scores indicate greater body appreciation.
Physical activity level and sedentary behaviorBaseline and 6 monthsPhysical activity and sedentary behavior will be assessed using the Physical Activity Questionnaire from the 2015 follow-up of the 1993 Pelotas Birth Cohort, which includes questions on leisure-time physical activity, active transportation, screen time, and sedentary behavior. Outcomes will be reported as time spent in physical activity and sedentary behaviors (minutes per week or hours per day), with higher physical activity indicating healthier behavior and higher sedentary time indicating less favorable behavior.
Participant's perception of the intervention6 monthsParticipants' perceptions of the intervention will be assessed through post-intervention semi-structured focus groups. Audio-recorded discussions will be transcribed and analyzed using thematic qualitative analysis to identify key themes related to participants' experiences, perceived benefits, and challenges of the intervention.

Countries

Brazil

Contacts

CONTACTBruno Gualano, PhD
gualano@usp.br+551130618789
CONTACTBruna Caruso Mazzolani, PhD
bruna.mazzolani@usp.br

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026