- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07558161
Positive Mirror Exposure for Body Image in Female Students With Disordered Eating
Efficacy of Repeated Positive Mirror Exposure in Enhancing Body Image and Affect Among Female University Students With Disordered Eating Symptoms
This study aims to examine the efficacy of repeated positive mirror exposure in improving body image and emotional affect among female university students with disordered eating symptoms. Disturbances in body image and negative affect are common among individuals experiencing disordered eating behaviors. Positive mirror exposure is a psychological intervention designed to promote body acceptance and reduce appearance-related distress by encouraging individuals to focus on neutral or positive aspects of their bodies during mirror viewing.
In this study, participants undergo repeated sessions of guided positive mirror exposure. Changes in body image and affect are assessed using standardized psychological measures before and after the intervention. The findings of this study are expected to contribute to the development of accessible and effective interventions for improving body image and emotional well-being in at-risk populations.
Study Overview
Status
Intervention / Treatment
Detailed Description
Disordered eating symptoms are frequently associated with body dissatisfaction and negative emotional states, particularly among young adult females. Body image disturbances are considered a core feature of disordered eating and are linked with increased psychological distress, including anxiety and depressive symptoms. Therefore, interventions targeting body image are critical in improving overall psychological well-being.
Positive mirror exposure is an emerging therapeutic approach that involves repeated and structured exposure to one's body in a mirror while encouraging non-judgmental or positive self-focused attention. Unlike traditional mirror exposure, which may focus on habituation to distress, positive mirror exposure emphasizes acceptance, appreciation, and cognitive restructuring of body-related thoughts.
The present study investigates the efficacy of repeated positive mirror exposure in enhancing body image and affect among female university students exhibiting disordered eating symptoms. Participants were assigned to an intervention protocol involving multiple sessions of guided mirror exposure. During these sessions, participants were instructed to observe their bodies and verbalize neutral or positive statements, with the aim of reducing negative self-evaluation and improving emotional responses.
Standardized self-report measures of body image and affect were administered before and after the intervention to assess changes over time. It is hypothesized that participants undergoing repeated positive mirror exposure will demonstrate significant improvements in body image and positive affect, along with reductions in negative affect.
The findings of this study may provide empirical support for a low-cost, easily implementable psychological intervention that can be applied in both clinical and non-clinical settings to address body image concerns and emotional distress associated with disordered eating.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Punjab Province
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Lahore, Punjab Province, Pakistan, 54000
- Kinnaird College for Women
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Female university students Aged between 18 and 25 years Presence of disordered eating symptoms as assessed by a screening measure Willingness to participate in mirror exposure sessions Ability to provide informed consent
Exclusion Criteria:
- Current diagnosis of a severe psychiatric disorder (e.g., psychosis, severe depression) Current treatment for an eating disorder Medical conditions affecting weight or eating behavior Inability to participate in intervention sessions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Full Positive Mirror Exposure
Participants received full positive mirror exposure involving guided observation of their entire body while verbalizing positive and accepting statements across repeated sessions.
|
A structured behavioral intervention involving repeated mirror exposure sessions in which participants observe their bodies and engage in guided verbalization of positive or neutral statements.
The intervention is designed to improve body image and emotional affect through increased body acceptance and reduced negative self-evaluation.
|
|
Experimental: Partial Positive Mirror Exposure
Participants received partial positive mirror exposure focusing on selected body areas with guided positive or neutral verbalizations during mirror viewing sessions.
|
A structured behavioral intervention involving repeated mirror exposure sessions in which participants observe their bodies and engage in guided verbalization of positive or neutral statements.
The intervention is designed to improve body image and emotional affect through increased body acceptance and reduced negative self-evaluation.
|
|
Active Comparator: Neutral Mirror Exposure
Participants engaged in neutral mirror exposure without emphasis on positive evaluation, serving as a comparison condition.
|
A structured behavioral intervention involving repeated mirror exposure sessions in which participants observe their bodies and engage in guided verbalization of positive or neutral statements.
The intervention is designed to improve body image and emotional affect through increased body acceptance and reduced negative self-evaluation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Positive and Negative Affect
Time Frame: Pre-intervention to post-intervention
|
Emotional affect will be measured using a standardized scale assessing positive and negative emotional states.
Changes in affect will be evaluated from pre- to post-intervention.
|
Pre-intervention to post-intervention
|
|
Body Image
Time Frame: Pre-intervention to post-intervention (e.g., baseline to 4 weeks)
|
Body image will be assessed using a standardized self-report measure evaluating participants' perceptions, attitudes, and satisfaction with their body.
Scores will be compared before and after the intervention to assess improvement.
|
Pre-intervention to post-intervention (e.g., baseline to 4 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Disordered Eating Symptoms
Time Frame: Pre-intervention to post-intervention (e.g., baseline to 4 weeks)
|
Disordered eating symptoms will be assessed using a standardized self-report measure evaluating behaviors and attitudes related to eating, including dietary restraint, binge eating tendencies, and concerns about weight and shape.
Changes in symptom levels will be compared before and after the intervention.
|
Pre-intervention to post-intervention (e.g., baseline to 4 weeks)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- OCD2026
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
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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