- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04677400
More Than Body Appearance (MBA) Intervention (MBA)
More Than Body Appearance (MBA) Intervention: Investigation of the Efficacy of a Psychological Online Intervention to Improve Body Image
The promotion of a positive body image is crucial to increase the efficacy of psychological interventions targeting body image. Recent studies indicated that positive body image also acts as a protective factor against the onset of ED symptoms. However, in the last decades, research has predominantly focused on reducing body dissatisfaction, with most available psychological interventions for body image adopting a disease reduction perspective while neglecting positive aspects of psychological functioning. This approach has shown limited efficacy in improving body image. Consequently, it is crucial to develop new psychological interventions including both perspectives (i.e., disease reduction and health promotion perspectives) to improve body image and to test their efficacy in different contexts and populations.
The aim of this study was to investigate the efficacy of a 2-week online psychological intervention (More than Body Appearance; MBA) designed to improve body image in young women at both high and low risk of developing Body Image Disorders and in female athletes practicing aesthetic sports.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
PD
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Padua, PD, Italy, 35131
- University of Padua
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 18 or above
Exclusion Criteria:
- Presence of a full-blown Body Image Disorder (BID);
- Current treatment for a BID.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
Participants in the Experimental group start the MBA intervention immediately (Time 0; T0).
|
The MBA is an online psychological intervention designed to improve body image. The intervention lasts 15 days, and it comprises two types of activity (1st and 2nd week). During the first week of the MBA intervention, participants sill read three blocks of psychoeducational material including information about: 1) body image; 2) positive body image and healthy lifestyles; and 3) body functionality. During the second week participants produce 3 structured writing assessment pertaining to body functionality and why it is important. Each assignment focused on two areas of body functionality: 1) body's senses and physical capacities; 2) health and creative skills; 3) self-care/daily routine and communication with others. For each writing assignment, participants were asked to reflect, describe, and specify why these aspects of body functionality were personally important and meaningful to them. |
|
Active Comparator: Waiting-list group
Participants in the waiting-list group start the MBA intervention at Time 1 (T1; 15 days after the Experimental group).
|
The MBA is an online psychological intervention designed to improve body image. The intervention lasts 15 days, and it comprises two types of activity (1st and 2nd week). During the first week of the MBA intervention, participants sill read three blocks of psychoeducational material including information about: 1) body image; 2) positive body image and healthy lifestyles; and 3) body functionality. During the second week participants produce 3 structured writing assessment pertaining to body functionality and why it is important. Each assignment focused on two areas of body functionality: 1) body's senses and physical capacities; 2) health and creative skills; 3) self-care/daily routine and communication with others. For each writing assignment, participants were asked to reflect, describe, and specify why these aspects of body functionality were personally important and meaningful to them. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body appreciation
Time Frame: 2 weeks
|
Improvements in body appreciation assessed by means of a self-report questionnaire: Body Appreciation Scale-2 (BAS-2; Minimum value: 10; Maximum value: 50; higher scores represent higher body appreciation)
|
2 weeks
|
|
Body dysmorphic disorder symptoms
Time Frame: 2 weeks
|
Reductions in body dysmorphic disorder symptoms assessed by means of a self-report questionnaire: Questionario sul Dismorfismo Corporeo (QDC; Minimum value: 40; Maximum value: 280; higher scores represent higher body dysmorphic disorder symptoms)
|
2 weeks
|
|
Functionality appreciation
Time Frame: 2 weeks
|
Improvements in functionality appreciation assessed by means of a self-report questionnaire: Functional Appreciation Scale (FAS; Minimum value: 7; Maximum value: 35; higher scores represent higher body functionality)
|
2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Risk of developing eating disorders
Time Frame: 2 weeks
|
Reductions of the risk of developing eating disorders assessed by means of a self-report questionnaire: Eating Disorder Inventory-3 (EDI-3; Minimum value: 25; Maximum value: 150; higher scores represent higher risk)
|
2 weeks
|
|
Intuitive eating
Time Frame: 2 weeks
|
Improvements in intuitive eating assessed by means of a self-report questionnaire: Intuitive Eating Sale-2 (IES-2; Minimum value: 23; Maximum value: 115; higher scores represent higher intuitive eating practices)
|
2 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Silvia Cerea, PhD, Department of General Psychology, University of Padova
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 3811
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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