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CompletedNCT02567890sBodyProjectUpdated Aug 5, 2019

Swedish Body Project for Prevention of Eating Disorders

An interventional study of Internet-based DBI and Expressive writing in Eating Disorders, sponsored by Karolinska Institutet. Completed at 1 site in Sweden. Open to female participants aged 15 Years to 20 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-08-05.

Sponsored by Karolinska Institutet · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
443
Allocation
Randomized
Ages
15 Years to 20 Years
Sex
Female
01

Study summary

Women in general and young girls in particular are constantly exposed to unhealthy body and appearance ideals through media that contribute to body dissatisfaction and unhealthy behaviors such as rigid dieting, which in interaction with genes and other factors increase the risk of developing eating disorders such as anorexia nervosa and bulimia nervosa. The investigators aim is to investigate the extent to which an interactive prevention program, delivered through Internet, called the Swedish Body Project (sBody Project) can decrease the emergence of eating disorders among young females. The sBody Project is based on a "Dissonance-Based Intervention: (DBI)" that has shown very promising results. The adaptations and changes in the format of delivery accomplished in this study might help to disseminate the program on a broad basis, and consequently affect the health of young females on a much larger scale the ever before.

Read the detailed description

OVERALL AIM AND RESEARCH QUESTIONS The overall aim of this project is to adapt the DBI to be implementable on a large scale by means of interactive groups working online, and new methods for easily and effectively training program facilitators), with recruitment using the model of social media (e.g., through various websites, collaborative projects, and blogs that are popular among the youth), and to evaluate the effect of the adapted version of the DBI. The program will remain interactive, and its effect can most probably be maintained over time to a higher degree than when implemented in its original format, as booster sessions can easily be included with no major problems in terms of logistics, meetings, allocation of participants, etc. The new format will also provide a framework for recruitment which reduces the risk of stigmatization.

Research questions

  1. How effective is the Internet-based DBI, immediately after the intervention and 6, 12, 18, and 24 months later, to reduce the onset of eating disorders?
  2. What channels in the Internet / social media leads to the best recruitment of the target group?
  3. Can further use and implementation of Internet-based DBI be maintained through a collaborative project (e.g., Wikipreventia) where the principles and methods of implementation (from the training of facilitators to recruitment, implementation and evaluation) are described, facilitated, and the experiences are accumulated?
  4. Is the adapted DBI cost-effective?
  5. Secondary questions concern the new format's potential for engaging the participants in booster sessions, degree of stigma in recruitment, mediators and moderators of outcome, and subgroup analyses.

STUDY DESIGN, MATERIAL AND METHODS Study Design The DBI will be adapted to be widely implemented and delivered via Internet and through a mobile "app", while maintaining its interactivity and underlying principles and theories. An initial evaluation of this model, although in a simpler format than what is proposed here, has shown promising results.

In a randomized trial, a total of at least 400 girls aged 15-18 with self-reported high levels of body dissatisfaction that is an established risk factor for the development of eating disorders will be randomized into three groups:

  1. Internet-based DBI, which consists of four interactive occasions, some homework assignments, and monitoring,
  2. Expressive Writing (placebo/attention control), and
  3. A wait-list control condition.

Those in the wait-list condition will randomized into one of the active interventions as soon as they have done a 6-month follow-up assessment. Direct and long-term effects of the interventions (6, 12, 18, and 24 months post-intervention) will be investigated by systematic measurements.

Study population and sample size Following the ethical guidelines from the Swedish Research Council, informed consent will be obtained, and an initial assessment (telephone interview) will be conducted. Those who meet the diagnostic criteria for any eating disorder, body dysmorphic disorder, or other serious conditions that require psychiatric care will be excluded. A booster session will be available every six months.

With an effect size of d=.32 between the DBI and the active control condition regarding the main outcome variable (eating disorder pathology), with three conditions in total, and at least 3 measurements (pre, post and 6-months follow-up) the investigators need at least 260 participants with p \< .05, an expected drop-out of 15%, and reliability of measures set between .75 and .95 to attain a power of at least .95. Given the recruitment channels, the investigators expect a much larger number than 260 to participate in the study, and to ensure adequate power for analyses using random effects and to take further drop-out over time into consideration the investigators aim for at least 400 participants.

Procedure Participants will be recruited through notes in different social media and the website of the project that will be linked to different fora which are known to engage adolescent girls. After obtaining informed consent, participants will be asked to download the "app" used for the study. Participants will then be asked to respond to the set of questionnaires (pre-intervention assessment) using a secure plattform, and they will be interviewed. They will then be asked to await feedback, and if included allocation to a group. Participants with significantly high scores on measures of depressive symptomatology or potential diagnosis of dysmorphophobia, eating disorders will be advised to seek professional help, and receive guidance on how to do it. The rest of the participants will be randomized to the study arms. They will then receive further information about their participations and use of the app.

The first session will be initiated by the facilitators who introduce basic issues about body image and the thin ideal.

The day before, and an hour before each meeting, the participants would receive a reminder.

The sessions will be each one hour long. The facilitators will guide the participants through the content of each session following a written manual. Participants who miss a session will be asked to listen to the recorded session ahead of the next session, and briefly discuss it with a facilitator.

Those randomized to Expressive Writing condition will be asked to reflect upon issues related to body image and self-concept according to a manual.

Participants will be asked to respond to the post-intervention assessment battery after the end of the fourth session. They will also be invited to participate in the booster sessions provided after the end of the intervention, and to respond to the follow-up assessments.

02

Conditions studied

  • Eating Disorders
03

In context

Feeding and Eating Disorders

740 studies on the registry are indexed under Feeding and Eating Disorders; 159 are open to participants now.

This study's enrollment of 443 is above the median of 75 across 540 interventional studies indexed under Feeding and Eating Disorders.

Browse Feeding and Eating Disorders studies →

Lead sponsor

Karolinska Institutet is the lead sponsor of 1,113 studies on the registry; 267 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
15 Years to 20 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Must have self-reported body dissatisfaction that is an established risk factor for the development of eating disorders.

Exclusion criteria

Exclusion Criteria:

  • Those who meet the diagnostic criteria for any eating disorder diagnosis, body dysmorphic disorder, or other serious conditions (e.g., bipolar disorders, schizophrenia) that require psychiatric care will be excluded.
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
443 participants (actual)

Study arms

  • Experimental
    Internet-based DBI

    Internet-based DBI, which consists of four interactive occasions, some homework assignments, and monitoring

    Behavioral: Internet-based DBI

  • Placebo comparator
    Expressive writing

    Expressive Writing (placebo/attention control) where participants write texts. This is the active control condition.

    Behavioral: Expressive writing

  • No intervention
    Waiting list

    A wait-list control condition.Those in the wait-list condition will not receive any treatment until they have done the 6-month follow-up assessment.

Interventions

  • BehavioralInternet-based DBI

    Participants will go through a four week interactive program that will improve body acceptance. Includes some homework assignments and monitoring.

    Also known as: sBody Project

  • BehavioralExpressive writing

    Participants will be asked to reflect upon issues related to body image.

06

What researchers measure

Primary outcomes

  1. Change in the occurrence of Eating disorder diagnosis

    Diagnostic interview to establish the diagnoses of eating disorders

    Time frame: 6 12, 18 and 24 months after the completed intervention that lasts 4 weeks

Secondary outcomes

  1. Composite EDE score

    Standardised and summed scores of the EDE diagnostic items

    Time frame: Pre-assessment, and 6, 12, and 24 months post intervention

  2. Self-reported ED symptoms based on the Eating Disorder Diagnostic Scale

    Global symptom severity

    Time frame: Pre-assessment, and 6, 12, 18, and 24 months post intervention

  3. Positive and Negative Affect

    Measured by the Positive and Negative Affect Schedule (PNAS),

    Time frame: Pre-assessment, and 6, 12, 18, and 24 months post intervention

  4. Restraint

    Restraint subscale of the Eating Disorders Examination Questionnaire

    Time frame: Pre-assessment, and 6, 12, 18, and 24 months post intervention

  5. Functional impairment due to eating disorder problems

    Measured by the Clinical Impairment Assessment

    Time frame: Pre-assessment, and 6, 12, 18, and 24 months post intervention

  6. Satisfaction and dissatisfaction with body parts

    Measured by the Body Parts Dissatisfaction Scale

    Time frame: Pre-assessment, and 6, 12, 18, and 24 months post intervention

  7. Internalization of the thin beauty ideal

    Measured by Ideal Body Stereotype Scale-revised

    Time frame: Pre-assessment, and 6, 12, 18, and 24 months post intervention

  8. Body shape dissatisfaction

    Measured by the Body Shape Questionnaire

    Time frame: Pre-assessment, and 6, 12, 18, and 24 months post intervention

07

Study locations

1 site
  • Karolinska Institutet
    Solna, 17177, Sweden
08

References and documents

Publications

  • Stice E, Shaw H. Eating disorder prevention programs: a meta-analytic review. Psychol Bull. 2004 Mar;130(2):206-27. doi: 10.1037/0033-2909.130.2.206. PubMed 14979770 ↗
  • Stice E, Rohde P, Durant S, Shaw H. A preliminary trial of a prototype Internet dissonance-based eating disorder prevention program for young women with body image concerns. J Consult Clin Psychol. 2012 Oct;80(5):907-16. doi: 10.1037/a0028016. Epub 2012 Apr 16. PubMed 22506791 ↗
  • Stice E, Schupak-Neuberg E, Shaw HE, Stein RI. Relation of media exposure to eating disorder symptomatology: an examination of mediating mechanisms. J Abnorm Psychol. 1994 Nov;103(4):836-40. doi: 10.1037//0021-843x.103.4.836. PubMed 7822589 ↗
  • Stice E, Shaw H, Becker CB, Rohde P. Dissonance-based Interventions for the prevention of eating disorders: using persuasion principles to promote health. Prev Sci. 2008 Jun;9(2):114-28. doi: 10.1007/s11121-008-0093-x. Epub 2008 May 28. PubMed 18506621 ↗
  • Stice E, Shaw H, Marti CN. A meta-analytic review of eating disorder prevention programs: encouraging findings. Annu Rev Clin Psychol. 2007;3:207-31. doi: 10.1146/annurev.clinpsy.3.022806.091447. PubMed 17716054 ↗
  • Stice E, Trost A, Chase A. Healthy weight control and dissonance-based eating disorder prevention programs: results from a controlled trial. Int J Eat Disord. 2003 Jan;33(1):10-21. doi: 10.1002/eat.10109. PubMed 12474195 ↗
  • White JH. Women and eating disorders, Part I: Significance and sociocultural risk factors. Health Care Women Int. 1992 Oct-Dec;13(4):351-62. doi: 10.1080/07399339209516013. PubMed 1478897 ↗
  • Welch E, Miller JL, Ghaderi A, Vaillancourt T. Does perfectionism mediate or moderate the relation between body dissatisfaction and disordered eating attitudes and behaviors? Eat Behav. 2009 Aug;10(3):168-75. doi: 10.1016/j.eatbeh.2009.05.002. Epub 2009 May 21. PubMed 19665100 ↗
  • Welch E, Lagerstrom M, Ghaderi A. Body shape questionnaire: psychometric properties of the short version (BSQ-8C) and norms from the general Swedish population. Body Image. 2012 Sep;9(4):547-50. doi: 10.1016/j.bodyim.2012.04.009. Epub 2012 Jun 19. PubMed 22721875 ↗
  • Welch E, Birgegard A, Parling T, Ghaderi A. Eating disorder examination questionnaire and clinical impairment assessment questionnaire: general population and clinical norms for young adult women in Sweden. Behav Res Ther. 2011 Feb;49(2):85-91. doi: 10.1016/j.brat.2010.10.010. Epub 2010 Nov 2. PubMed 21185552 ↗
  • Treasure J, Macare C, Mentxaka IO, Harrison A. The use of a vodcast to support eating and reduce anxiety in people with eating disorder: A case series. Eur Eat Disord Rev. 2010 Nov-Dec;18(6):515-21. doi: 10.1002/erv.1034. PubMed 20669153 ↗
  • Ghaderi A, Stice E, Andersson G, Eno Persson J, Allzen E. A randomized controlled trial of the effectiveness of virtually delivered Body Project (vBP) groups to prevent eating disorders. J Consult Clin Psychol. 2020 Jul;88(7):643-656. doi: 10.1037/ccp0000506. PubMed 32551736 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 5, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02567890
Lead sponsor
Karolinska Institutet
Collaborators
Linkoeping University, Oregon Research Institute
Responsible party
Ata Ghaderi (Professor, Karolinska Institutet) — Principal investigator
First posted
Oct 5, 2015
Start date
Sep 2015
Primary completion
Jun 28, 2019
Completion
Jun 28, 2019
Last update
Aug 5, 2019

Study contacts

Ata Ghaderi, PhD
principal investigator · Karolinska Institutet

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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