Comparing self-compassion and diet approaches for body dissatisfaction and disordered eating in women
Comparison of Nutritional Counseling Based on Self-compassion Vs. Diet Approach on Body Dissatisfaction, Food Restriction, and Disordered Eating in Adult Women
This study is testing whether a self-compassion approach to nutrition can help women feel better about their bodies and reduce disordered eating compared to a traditional diet plan.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 76 (estimated) |
| Ages | 25 Years to 59 Years |
| Sex | Female |
| Sponsor | Hospital de Clinicas de Porto Alegre Academic / other |
| Locations | 1 site (Porto Alegre, RS) |
| Trial ID | NCT06084260 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to evaluate the effectiveness of nutritional counseling based on self-compassion techniques compared to a traditional diet approach in addressing body dissatisfaction and disordered eating among women. Adult women aged 25 to 59 will be randomly assigned to either the self-compassion group or the diet group, participating in weekly one-hour sessions over eight weeks. The study will measure outcomes such as body dissatisfaction, disordered eating behaviors, and self-compassion levels using validated questionnaires. Data analysis will involve statistical tests to determine the differences between the two approaches.
Who should consider this trial
Good fit: Ideal candidates for this study are adult women aged 25 to 59 who experience body dissatisfaction and have access to communication apps.
Not a fit: Patients with diagnosed mood disorders, eating disorders, or significant non-communicable diseases may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a more effective and compassionate approach to improving body image and reducing disordered eating behaviors in women.
How similar studies have performed: While the concept of self-compassion in addressing body image issues is gaining traction, this specific comparative approach is relatively novel and has not been extensively tested in clinical settings.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * age between 25 and 59 years; * access to cell phone and communication apps. Exclusion Criteria: * diagnosis of depression, mood disorders (anxiety, bipolar, borderline), eating disorders, or a history of suicidal ideation; * diagnosis of non-communicable diseases such as diabetes, kidney disease, cardiovascular or neurological diseases.
Where this trial is running
Porto Alegre, RS
- Hospital de Clínicas de Porto Alegre — Porto Alegre, Rs, Brazil (Recruiting)
Study contacts
- Principal investigator: Carolina G de Souza, PhD — Hospital de Clínicas de Porto Alegre
- Study coordinator: Alessandra B Ramos
- Email: alessandrabehar@gmail.com
- Phone: 5551998191636
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.