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N/A N=46 Treatment

Targeting Body Image Among Women of Higher Body Weight

Obesity · Overweight · Body Image

Enrolled (actual)
46
Serious AEs
0.0%
Results posted
Jun 2023
Primary outcome: Primary: EDE-Q Weight and Shape Concern — 3; 6; 0; 3 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Body Project (Behavioral)
Age
Adult, Older Adult · 25+ yrs
Sex
Female
Sponsor
The Miriam Hospital
Primary completion
May 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
EDE-Q Weight and Shape Concern
3; 6; 0; 3; 4; 5
PRIMARY
Sociocultural Attitudes Towards Appearance Questionnaire-4
3.98; 3.2; 3.2; 3.26; 3.6; 3.8
PRIMARY
Weight Bias Internalization Scale
5.84; 5.09; 5.6; 5.0; 5.53; 5.37
SECONDARY
Momentary Weight and Shape Concern
6; 5; 7; 6; 6; 3
SECONDARY
Qualitative Feedback
8; 6; 4; 5; 3

Summary

The goal of this study is to modify the evidence-based Body Project intervention to more powerfully target weight and shape concern among women with BMI between 25-40 using exploratory sequential mixed methodology (using both quantitative and focus group data). Initial modifications to the intervention will be made to incorporate content targeting weight stigma and to ensure the materials are developmentally appropriate for adult women. Then a small group (n=5-10) of women with high weight and shape concern will receive the 4 week body project intervention; we will collect pre-post questionnaire data on weight and shape concern, thin ideal and weight stigma, and use ecological momentary assessment to examine in-the-moment thoughts about weight and shape. The body project intervention will then be revised using this information in combination with participant feedback elicited during a focus group session. The next iteration of the intervention will then be tested in another small group of n=5-10; it is estimated that it will take 4-6 iterations to achieve a more robust intervention program that is acceptable to the target sample. Subgroups (race/ethnicity, BMI class) will be evaluated to ensure suitability across groups.

Eligibility Criteria

Inclusion Criteria

  • Female
  • BMI between 25-40
  • EDE-Q weight concern subscale>4
  • EDE-Q shape concern subscale>4.25
  • Personal use of cell phone
  • Able to engage in moderate intensity activity
  • Desire for weight loss

Exclusion Criteria

  • No eating disorder history
  • Not pregnant
  • Not breastfeeding
  • No delivery within 9 months
  • No substance abuse disorder
  • No weight loss medication or history of bariatric surgery
  • No other weight loss program participation
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04810247). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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