Disordered Eating BehaviorsNCT07149324
Can a Single-session Intervention Decrease Risk for Mental Health Symptoms in Young Adults? A Preliminary Investigation of Feasibility and Acceptability
A study testing Single Session for Overevaluation in people with Disordered Eating Behaviors and Disordered Eating, run by Chloe White at 1 site in Canada.
Trial summary
This project has two primary aims: 1) to develop a single session intervention to understand different forms of self-evaluation with input from young adults, and 2) to examine whether a single session can improve the ways in which young adults measure their self-importance with a session led by a trained masters-level… Read more about this study
- Who is it for?
- Ages 18 to 25 yearsHealthy volunteers can take part
- Conditions the study is for
- Disordered Eating Behaviors, Disordered Eating
- What is being tested?
- Single Session for Overevaluation
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 15 participants
- Where
- 1 siteCanada
- Study dates
- Nov 2025to Sep 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 25 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- between 18-25 years of age
- English speaking
- Demonstrate elevated overevaluation of weight, shape or muscularity
Who cannot join
- Have or have had in the past an eating disorder
- Is receiving treatment for an eating disorder
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Shannon Zaitsoff, PhD contact
Canada1 site
Simon Fraser University
Burnaby, British Columbia
Chloe L White, M.A., +1-778-782-9022, chloe_white@sfu.ca
Shannon Zaitsoff, Assistant Professor, PhD
About this study
Official title: Can a Single Session Intervention Decrease Eating Disorder Symptoms in At-risk University Students? A Pilot Study.
This project has two primary aims: 1) to develop a single session intervention to understand different forms of self-evaluation with input from young adults, and 2) to examine whether a single session can improve the ways in which young adults measure their self-importance with a session led by a trained masters-level therapist. Eligible participants will complete a baseline questionnaire, a therapeutic session online, and follow-up questionnaires.
Read the detailed description
PURPOSE:
The purpose of the present study is to 1) seek input from young adults regarding the utility, content and structure of a single session intervention, and 2) to examine whether a single session can alter mental health symptoms in young adults. Specifically, the study will seek to examine how intervening with a core risk factor of disordered eating and low mood, self-evaluation based in appearance, may influence mental health symptoms, including self-esteem, low mood, disordered eating, and body satisfaction.
JUSTIFICATION:
This study is important for various reasons. Basing one's self-esteem nearly exclusively on appearance-related variables (e.g., shape, weight) is a risk factor for negative mental health symptoms, such as disordered eating, low mood, and diminished self-esteem. Thus, self-esteem based on appearance may be an important place to intervene to decrease potential negative mental health outcomes and increase resiliency. However, interventions which are designed to treat over reliance on appearance in evaluating one's self-esteem range between 16-20 sessions in duration and are often time and cost inefficient to provide to all individuals who evaluate themselves based on their appearance; and importantly, single session interventions have been shown to increase mood, healthy eating behaviours, and body satisfaction in young adults and adolescents. Thus, there exists a need for highly specific and specialized interventions which are informed by known past risk factors, such as overevaluation of appearance. Thus, development and testing of a single session intervention developed through consideration of research on interventions for disordered eating, low mood, and diminished self-esteem to date, and through consult with overevaluation of appearance, is a critical development to diminish the overall negative health consequences of a dysfunctional system of self-evaluation.
Given the paucity of research conducted on this specific topic to date, the present study will conduct two phases of the same study to examine a novel single session intervention to change how participants measure their self-importance. A checklist outlining the various components of the intervention session is in the Support Documents section. In brief, the intervention session will begin with individuals completing a modified version of the Shape and Weight-Based Self-Esteem Inventory (SAWBS) to assess their self-reliance on (overevaluation of) appearance. After completing this measure, participants and the clinician will discuss the participants overevaluation in reference to the average levels of overevaluation of other individuals their age. Additionally, the clinician will provide psychoeducation about their overevaluation in reference to the individual's risk for negative mental health outcomes (e.g., low mood, disordered eating, anxiety). Importantly, discussions and psychoeducation will be tailored by the therapist to intervene specifically with symptoms that are identified as the most concerning by the participant. Following this discussion, participants will complete a reflective writing exercise, complete the SAWBS again indicating which areas bring them pleasure that they would like to increase, and come up with a plan of action to enhance reliance on other areas that are important to them.
Recruitment will occur in two phases. Phase I will be focused on intervention development. In Phase I, five eligible participants will receive the intervention session, followed by two brief interviews designed to gather feedback about the intervention session. Importantly, these interviews will be led by trained research assistants who have completed masters in Clinical Psychology rather than the lead therapist. In these interviews, participants will be asked about their experience of the session, whether they would change anything about the session, their preference for duration or structure of the session, and will be provided with open-ended opportunities to discuss anything else relevant to their experience in the study. They will also complete a secondary interview one week following the intervention, which will include open-ended questions about the efficacy of the session over the past week and provide them with a second opportunity to provide feedback about the session content. This phase will also include a series of measures completed at pre-intervention, including demographic questions. Additionally, some measures will be completed at post-intervention (measures in Supported Documents). The measures completed will be a well-validated measure of disordered eating symptoms (the Eating Disorder-15), select questions from the Eating Disorder Examination-Questionnaire (EDE-Q), a measure of overevaluation of appearance (Shape and Weight Based Self-Esteem Inventory), a quantitative measure of session acceptability (Program Feedback Scale), a measure of body satisfaction (BSS; ), and a measure of mood (BHS-4). Importantly, adequate acceptability of the intervention, demonstrated via responses on the Program Feedback Scale of equal to or >3.5/5, and qualitative interviews (interview questions provided in Supported Documents) will need to be demonstrated across participants to proceed with Phase II.
Phase II will be a case series study, with the goal of examining the utility of the single session intervention at modifying how participants measure their self-importance over a four-week period. A case series will be used to capitalize on the relatively rare population of individuals with demonstrated heightened overvaluation of appearance. Additionally, a case series study will allow researchers to develop increasingly fine-grained hypotheses about the feasibility of a single session intervention for intervening with over reliance on appearance in self-evaluation, a presently unknown possibility. In Phase II, ten eligible participants will receive the intervention session, followed by two brief follow-up questionnaires. These participants will complete a pre-intervention questionnaire, a post-intervention questionnaire, a one-week follow-up questionnaire, and a four-week follow-up questionnaire. In the pre-intervention questionnaire, participants will provide demographic information and will complete a well-validated measure of disordered eating (the Eating Disorder-15), select questions from the Eating Disorder Examination-Questionnaire (EDE-Q), as well as measures of overevaluation of appearance (Shape and Weight Based Self-Esteem Inventory), body shape satisfaction, and low mood. In the post-intervention questionnaire, they will complete the body shape satisfaction scale, select questions from the Eating Disorder Examination-Questionnaire (EDE-Q), the measure of mood (BHS-4), and a measure of session acceptability (Program Feedback Scale, PFS). The one-week follow-up will include the measure of disordered eating symptoms (ED-15 \& EDE-Q), body shape satisfaction, and the measure of mood. The four-week follow-up will include the measure of disordered eating, body shape satisfaction, mood, and overevaluation of appearance. Each participant will be prompted to respond to 1- and 4-week follow-up questionnaires via their preferred method of contact (email or text message).
STATISTICAL ANALYSES:
Statistical analyses will be descriptive in nature given the treatment development and case series design. These designs do not require large sample sizes and increase focus on patterns within participants, rather than between. Thus, inferential statistics are not used and no apriori power analyses were conducted. Alternatively, to determine sample size, a careful surveillance of literature on case series studies and treatment development was undertaken. Analyses for Phase I will include examining the qualitative feedback given by the five participants regarding the session content for themes and examination of the Program Feedback Scale item-level responses across participants through measures of central tendency (e.g., mean). Analyses for Phase II will examine trends of the ten participant scores across measures using measures of central tendency and plotting various data points on graphs. All measures, including mood, disordered eating, overevaluation, body shape satisfaction, and the program feedback scale will be examined using these techniques for all participants.
- Conditions
- Disordered Eating Behaviors, Disordered Eating
- Being tested
- Single Session for Overevaluation
- Keywords
- Eating disorders, Depression, Self-esteem
- Medical subject headings
- Disordered Eating Behavior, Feeding and Eating Disorders, Depression
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Single Session for OverevaluationBehavioural
A single session informed by the principles of Cognitive Behavioural Therapy-Enhanced and motivational intervening.
| Study group | Role | What they receive |
|---|---|---|
| Intervention Group | Other | Not described Receives: Behavioral: Single Session for Overevaluation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Shape and Weight Based Self-Esteem Inventory (SAWBS)
Pie graph between 0-100. Higher scores indicate greater overevaluation of shape, weight or muscularity.
Measured: From enrollment to the end of follow-up at 4-weeks
Eating Disorder-15 (ED-15)
The ED-15 is comprised of 15 questions and uses a 7-point rating scale (0 - 6) for each item, with higher scores suggesting a greater likelihood or presence of eating disorder symptoms.
Measured: From enrollment to the end of follow-up at 4-weeks
Eating Disorder Examination - Questionnaire (EDE-Q)
The EDE-Q is comprised of 28 questions and uses a 7-point rating scale (0-6) for each item, with higher scores reflecting greater ED symptoms.
Measured: From enrollment to the end of follow-up at 4-weeks
Program Feedback Scale (PFS)
The PFS is a 9-item questionnaire which was developed to examine acceptability of SSI's. Items one through seven are rated on a 5-point Likert-type scales ranging from 0 (really disagree) to 4 (really agree). Higher scores indicate greater acceptability of the single session. The remaining two items are open-ended questions (e.g., "What did you like about the program?") which allow for participants to provide detailed feedback.
Measured: Immediately after the intervention
Secondary outcomes (2)
Beck Hopelessness Scale-4 (BHS-4)
The BHS-4 is a 4-item measure asking participants to rate their sense of hopelessness using a 4-item Likert-type scale. A total score is formed from summing across all 4-items to form an overall total score which signifies the extent to which the individual is experiencing hopelessness; thus, a higher score indicates greater depressive symptoms.
Measured: From enrollment to the end of follow-up at 4-weeks
Body Shape Satisfaction Scale - 10 (BSS-10)
The Body Shape Satisfaction Scale - 10 is an abbreviated version of the Body Shape Satisfaction Scale. The 10-item questionnaire uses a 5-point Likert type scale, ranging from 1 (very dissatisfied) to 5 (very satisfied), to indicate the extent to which participants are satisfied with different parts of their bodies. Higher scores indicate greater satisfaction with different body parts.
Measured: From enrollment to the end of treatment at 4-weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Sep 2025
- Study startNov 2025 (estimated)
- Primary completionAug 2026 (estimated)
- Study completionSep 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Disordered Eating BehaviorsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- This will be a case series study.
- Masking
- None (open label)
- Enrolment
- 15 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Chloe White
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Chloe White, Simon Fraser University
- Investigators
- Shannon Zaitsoff, PhD, Principal investigator, Simon Fraser University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07149324
- Sponsor's protocol ID
- 518585
- Status last verified
- Aug 2025
- First submitted
- 23 Jul 2025
- Last updated
- 12 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Anonymized data of measures used in the study will be shared.
Publications
White C, Maraun M, Zaitsoff S. How do I evaluate myself? The importance of examining overevaluation of muscularity in risk for eating disorder symptoms. J Eat Disord. 2025 Oct 23;13(1):233. doi: 10.1186/s40337-025-01419-3.
PubMed 41131650
Study at a glance
From the registry record, last updated by the sponsor on 12 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Can a Single Session Intervention Decrease Eating Disorder Symptoms in At-risk University Students? A Pilot Study.
- ClinicalTrials.gov ID
- NCT07149324
- Acronym / sponsor ID
- 518585
- Conditions
- Disordered Eating Behaviors, Disordered Eating
- Keywords
- Eating disorders, Depression, Self-esteem
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 15 participants (estimated)
- Lead sponsor
- Chloe WhiteUniversity, hospital or other
- Study start
- Nov 2025 (estimated)
- Primary completion
- Aug 2026 (estimated)
- Study completion
- Sep 2026 (estimated)
- First posted
- 2 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This project has two primary aims: 1) to develop a single session intervention to understand different forms of self-evaluation with input from young adults, and 2) to examine whether a single session can improve the ways in which young adults measure their self-importance with a session led by a trained masters-level therapist. Eligible participants will complete a baseline questionnaire, a therapeutic session online, and follow-up questionnaires.
Detailed description
PURPOSE:
The purpose of the present study is to 1) seek input from young adults regarding the utility, content and structure of a single session intervention, and 2) to examine whether a single session can alter mental health symptoms in young adults. Specifically, the study will seek to examine how intervening with a core risk factor of disordered eating and low mood, self-evaluation based in appearance, may influence mental health symptoms, including self-esteem, low mood, disordered eating, and body satisfaction.
JUSTIFICATION:
This study is important for various reasons. Basing one's self-esteem nearly exclusively on appearance-related variables (e.g., shape, weight) is a risk factor for negative mental health symptoms, such as disordered eating, low mood, and diminished self-esteem. Thus, self-esteem based on appearance may be an important place to intervene to decrease potential negative mental health outcomes and increase resiliency. However, interventions which are designed to treat over reliance on appearance in evaluating one's self-esteem range between 16-20 sessions in duration and are often time and cost inefficient to provide to all individuals who evaluate themselves based on their appearance; and importantly, single session interventions have been shown to increase mood, healthy eating behaviours, and body satisfaction in young adults and adolescents. Thus, there exists a need for highly specific and specialized interventions which are informed by known past risk factors, such as overevaluation of appearance. Thus, development and testing of a single session intervention developed through consideration of research on interventions for disordered eating, low mood, and diminished self-esteem to date, and through consult with overevaluation of appearance, is a critical development to diminish the overall negative health consequences of a dysfunctional system of self-evaluation.
Given the paucity of research conducted on this specific topic to date, the present study will conduct two phases of the same study to examine a novel single session intervention to change how participants measure their self-importance. A checklist outlining the various components of the intervention session is in the Support Documents section. In brief, the intervention session will begin with individuals completing a modified version of the Shape and Weight-Based Self-Esteem Inventory (SAWBS) to assess their self-reliance on (overevaluation of) appearance. After completing this measure, participants and the clinician will discuss the participants overevaluation in reference to the average levels of overevaluation of other individuals their age. Additionally, the clinician will provide psychoeducation about their overevaluation in reference to the individual's risk for negative mental health outcomes (e.g., low mood, disordered eating, anxiety). Importantly, discussions and psychoeducation will be tailored by the therapist to intervene specifically with symptoms that are identified as the most concerning by the participant. Following this discussion, participants will complete a reflective writing exercise, complete the SAWBS again indicating which areas bring them pleasure that they would like to increase, and come up with a plan of action to enhance reliance on other areas that are important to them.
Recruitment will occur in two phases. Phase I will be focused on intervention development. In Phase I, five eligible participants will receive the intervention session, followed by two brief interviews designed to gather feedback about the intervention session. Importantly, these interviews will be led by trained research assistants who have completed masters in Clinical Psychology rather than the lead therapist. In these interviews, participants will be asked about their experience of the session, whether they would change anything about the session, their preference for duration or structure of the session, and will be provided with open-ended opportunities to discuss anything else relevant to their experience in the study. They will also complete a secondary interview one week following the intervention, which will include open-ended questions about the efficacy of the session over the past week and provide them with a second opportunity to provide feedback about the session content. This phase will also include a series of measures completed at pre-intervention, including demographic questions. Additionally, some measures will be completed at post-intervention (measures in Supported Documents). The measures completed will be a well-validated measure of disordered eating symptoms (the Eating Disorder-15), select questions from the Eating Disorder Examination-Questionnaire (EDE-Q), a measure of overevaluation of appearance (Shape and Weight Based Self-Esteem Inventory), a quantitative measure of session acceptability (Program Feedback Scale), a measure of body satisfaction (BSS; ), and a measure of mood (BHS-4). Importantly, adequate acceptability of the intervention, demonstrated via responses on the Program Feedback Scale of equal to or >3.5/5, and qualitative interviews (interview questions provided in Supported Documents) will need to be demonstrated across participants to proceed with Phase II.
Phase II will be a case series study, with the goal of examining the utility of the single session intervention at modifying how participants measure their self-importance over a four-week period. A case series will be used to capitalize on the relatively rare population of individuals with demonstrated heightened overvaluation of appearance. Additionally, a case series study will allow researchers to develop increasingly fine-grained hypotheses about the feasibility of a single session intervention for intervening with over reliance on appearance in self-evaluation, a presently unknown possibility. In Phase II, ten eligible participants will receive the intervention session, followed by two brief follow-up questionnaires. These participants will complete a pre-intervention questionnaire, a post-intervention questionnaire, a one-week follow-up questionnaire, and a four-week follow-up questionnaire. In the pre-intervention questionnaire, participants will provide demographic information and will complete a well-validated measure of disordered eating (the Eating Disorder-15), select questions from the Eating Disorder Examination-Questionnaire (EDE-Q), as well as measures of overevaluation of appearance (Shape and Weight Based Self-Esteem Inventory), body shape satisfaction, and low mood. In the post-intervention questionnaire, they will complete the body shape satisfaction scale, select questions from the Eating Disorder Examination-Questionnaire (EDE-Q), the measure of mood (BHS-4), and a measure of session acceptability (Program Feedback Scale, PFS). The one-week follow-up will include the measure of disordered eating symptoms (ED-15 \& EDE-Q), body shape satisfaction, and the measure of mood. The four-week follow-up will include the measure of disordered eating, body shape satisfaction, mood, and overevaluation of appearance. Each participant will be prompted to respond to 1- and 4-week follow-up questionnaires via their preferred method of contact (email or text message).
STATISTICAL ANALYSES:
Statistical analyses will be descriptive in nature given the treatment development and case series design. These designs do not require large sample sizes and increase focus on patterns within participants, rather than between. Thus, inferential statistics are not used and no apriori power analyses were conducted. Alternatively, to determine sample size, a careful surveillance of literature on case series studies and treatment development was undertaken. Analyses for Phase I will include examining the qualitative feedback given by the five participants regarding the session content for themes and examination of the Program Feedback Scale item-level responses across participants through measures of central tendency (e.g., mean). Analyses for Phase II will examine trends of the ten participant scores across measures using measures of central tendency and plotting various data points on graphs. All measures, including mood, disordered eating, overevaluation, body shape satisfaction, and the program feedback scale will be examined using these techniques for all participants.
Study design
- Primary purpose
- Prevention
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- This will be a case series study.
| Arm | Type | Receives |
|---|---|---|
| Intervention Group | Other | Behavioral: Single Session for Overevaluation |
Who may qualify
- Ages
- 18 to 25 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- between 18-25 years of age
- English speaking
- Demonstrate elevated overevaluation of weight, shape or muscularity
Key exclusion criteria (2 listed)
- Have or have had in the past an eating disorder
- Is receiving treatment for an eating disorder
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Single Session for OverevaluationA single session informed by the principles of Cognitive Behavioural Therapy-Enhanced and motivational intervening. | Behavioural | Intervention Group |
Primary outcome
Shape and Weight Based Self-Esteem Inventory (SAWBS)
Time frame: From enrollment to the end of follow-up at 4-weeks
Pie graph between 0-100. Higher scores indicate greater overevaluation of shape, weight or muscularity.
Eating Disorder-15 (ED-15)
Time frame: From enrollment to the end of follow-up at 4-weeks
The ED-15 is comprised of 15 questions and uses a 7-point rating scale (0 - 6) for each item, with higher scores suggesting a greater likelihood or presence of eating disorder symptoms.
Eating Disorder Examination - Questionnaire (EDE-Q)
Time frame: From enrollment to the end of follow-up at 4-weeks
The EDE-Q is comprised of 28 questions and uses a 7-point rating scale (0-6) for each item, with higher scores reflecting greater ED symptoms.
Program Feedback Scale (PFS)
Time frame: Immediately after the intervention
The PFS is a 9-item questionnaire which was developed to examine acceptability of SSI's. Items one through seven are rated on a 5-point Likert-type scales ranging from 0 (really disagree) to 4 (really agree). Higher scores indicate greater acceptability of the single session. The remaining two items are open-ended questions (e.g., "What did you like about the program?") which allow for participants to provide detailed feedback.
2 secondary outcomes
Beck Hopelessness Scale-4 (BHS-4)
Time frame: From enrollment to the end of follow-up at 4-weeks
Body Shape Satisfaction Scale - 10 (BSS-10)
Time frame: From enrollment to the end of treatment at 4-weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Sep 2025.
- Background: PubMed 41131650White C, Maraun M, Zaitsoff S. How do I evaluate myself? The importance of examining overevaluation of muscularity in risk for eating disorder symptoms. J Eat Disord. 2025 Oct 23;13(1):233. doi: 10.1186/s40337-025-01419-3.
- Online SAWBSLink provided by the sponsor.
- Individual participant dataSharing planned: Yes. Anonymized data of measures used in the study will be shared.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Shannon Zaitsoff, PhD contact
Shannon Zaitsoff, PhD principal investigator
Simon Fraser University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Single Session for Overevaluation in people with Disordered Eating Behaviors and Disordered Eating, run by Chloe White at 1 site in Canada.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 12 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Chloe White, M.A. ((778) 782-9022, chloe_white@sfu.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Shape and Weight Based Self-Esteem Inventory (SAWBS) (time frame: From enrollment to the end of follow-up at 4-weeks). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07149324, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Sep 2025; AzTrials last refreshed its copy on 28 Oct 2026.