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Reducing Suicide Risk Associated With Weight Loss

Reducing Suicide Risk Associated With Weight Loss

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03541824
Enrollment
59
Registered
2018-05-31
Start date
2016-07-01
Completion date
2017-03-20
Last updated
2018-05-31

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

Conditions

Eating Behavior, Self Harm, Weight Loss

Brief summary

The purpose of this study is to examine the efficacy of an intervention aimed at promoting a healthy lifestyle and reducing risk factors associated with eating pathology, nonsuicidal self-injury, and suicidal behavior. We are also interested in assessing whether this intervention has the potential to prevent future symptoms of eating problems and self-harm urges and behaviors. The broader goal of this research is to identify factors that may help us better understand the prevention of self-harm behaviors and develop more effective treatments for these problems.

Detailed description

The current study was designed as a proof-of-concept study to test the association between weight suppression (WS; difference between one's highest and lowest weight) and non-suicidal self-injury (NSSI). Previous research has found an association between current WS and lifetime NSSI and that this association was mediated by depressive symptoms and drive for thinness. The current study therefore modified an existing online cognitive dissonance-based program (the e-Body Project) using mixed gender content (from the Body Project 4 All scripts) to target posited mediators, i.e., depressive symptoms and weight and shape concerns, in a sample of individuals with WS and engagement in current NSSI.

Interventions

The Body Acceptance Program is a mixed-gender modification of the eBody Project, an online intervention in which cognitive dissonance principals are used to reduce eating pathology.

Sponsors

Florida State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-65 years old * At least 5 pounds weight suppression * Engaged in non-suicidal self-injury at least once in past month

Exclusion criteria

* Indicated being sure of suicide attempt on eligibility screener * Live outside of the United States * Currently pregnant

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline on the Self-Injurious Thoughts and Behaviors Interview-Short Form (self-report) at follow-upPre-assessment and post-assessment (after intervention or two weeks from baseline)Self-harm frequency and likelihood

Secondary

MeasureTime frameDescription
Change from baseline on the Body Esteem Scale: Weight subscale at follow-upPre-assessment and post-assessment (after intervention or two weeks from baseline)Feelings about one's weight; scores are summed and range from 0-32, higher scores indicate greater weight esteem
Change from baseline on the Body Esteem Scale: Attribution subscale at follow-upPre-assessment and post-assessment (after intervention or two weeks from baseline)Feelings about one's characteristics; scores are summed and range from 0-20, higher scores indicate greater self-esteem
Change from baseline on the Body Esteem Scale: Appearance subscale at follow-upPre-assessment and post-assessment (after intervention or two weeks from baseline)Feelings about one's appearance; scores are summed and range from 0-40, higher scores indicate greater appearance esteem
Change from baseline on the Body Shape Questionnaire (8-item version #3) at follow-upPre-assessment and post-assessment (after intervention or two weeks from baseline)Assessment of weight and shape concerns
Change from baseline on the Positive and Negative Affect Schedule at follow-upPre-assessment and post-assessment (after intervention or two weeks from baseline)Captures current positive and negative affect
Change from baseline on the Beck Depression Inventory II at follow-upPre-assessment and post-assessment (after intervention or two weeks from baseline)Depressive symptoms

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026