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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ISRCTN |
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Last refreshed on:
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22 March 2021 |
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Main ID: |
ISRCTN13716228 |
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Date of registration:
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26/02/2016 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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everyBody – Tailored online health promotion and eating disorder prevention for women at different risk stages
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Scientific title:
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Tailored online health promotion and eating disorder prevention for women at different risk stages aiming to reduce weight and shape concerns |
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Date of first enrolment:
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16/11/2016 |
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Target sample size:
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4160 |
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Recruitment status: |
Completed |
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URL:
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http://isrctn.com/ISRCTN13716228 |
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Study type:
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Interventional |
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Study design:
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Single centre non-randomized parallel group interventional study (Prevention)
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Phase:
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Not Applicable
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Countries of recruitment
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Austria
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Germany
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Luxembourg
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Switzerland
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Contacts
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Name:
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Address:
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Telephone:
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Email:
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Affiliation:
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Name:
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Corinna
Jacobi |
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Address:
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Technische Universität Dresden
Klinische Psychologie und Psychotherapie
Chemnitzer Straße 46a
01187
Dresden
Germany |
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Telephone:
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+49 351 463 38576 |
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Email:
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corinna.jacobi@tu-dresden.de |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria:
1. Age 18 or older
2. Female
3. Access to Internet
4. Informed consent (online)
Exclusion criteria:
1. Individuals reporting binge eating and/or compensatory behaviours more than once a week
2. Underweight individuals (BMI less than 18.5)
Age minimum:
Age maximum:
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Eating disorders
Mental and Behavioural Disorders
Eating disorders
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Intervention(s)
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Based on the individual screening result, participants will be allocated to one of the five parallel intervention groups. Women with full-syndrome eating disorders will be excluded from participation and receive a treatment referral. Following informed consent and baseline assessment of primary and secondary outcomes each group obtains access to an evidence-based online prevention program tailored to their respective needs and conditions: everyBody Original, everyBody Basic, everyBody Plus, everyBody AN and everyBody Fit. All programs offer psychoeducation and behavioral exercises aiming to promote or establish healthy eating and exercise habits as well as improve self-esteem.
EveryBody Original targets women with a BMI from 21 to 25 who report elevated weight and shape concerns, but no other symptoms of an eating disorder. Participants from this group receive 8 weekly intervention sessions and get access to a moderated group discussion board. An additional aim in this group is the improvement of body image.
EveryBody Plus targets women with a BMI greater than 18.5 who report occasional binge eating and/or compensatory behaviors. Participants from this group receive 8 weekly intervention sessions, get access to a moderated group discussion board and receive weekly personal feedback. Additional aims in this group are the reduction of binge eating and/or purging and improvement of body image.
EveryBody AN targets women with a BMI ranging from 18.5 to 21 who report elevated weight and shape concerns but no other eating disorder symptoms. Participants from this group receive 10 weekly intervention sessions, get access to a moderated group discussion board and receive weekly personal feedback. Additional aim
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Primary Outcome(s)
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Weight and shape concerns (measured with Weight Concerns Scale) at baseline and post-intervention
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Secondary Outcome(s)
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1. Weight and shape concerns are measured using the Weight Concerns Scale at baseline, 6 and 12 months follow up (effectiveness)
2. Core eating disorder symptoms (binge eating, compensatory behaviors are measured by self-report (questionnaire) at baseline, post-intervention, 6 and 12 months follow up (effectiveness)
3. Self-esteem is measured using the Rosenberg Self Esteem-Scale at baseline, post intervention, 6 and 12 months follow up
4. Quality of life is measured using the Assessment of Quality of Life-8D questionnaire at baseline, post intervention, 6 and 12 months follow up
5. The reach of the program is measured using sociodemographic variables (questionnaire) of participants at baseline
6. The adoption of the program is measured qualitatively by analyzing communication with stakeholders pre-intervention
7. The implementation of the program is measured by analyzing access paths, cost per recruit and participants adherence to the program before, during and post intervention
8. The maintenance of the program on a participant level is measured by assessing primary and secondary effectiveness outcomes
9. The maintenance of the program on a setting level is qualitatively assessed by analyzing stakeholder attempts to deliver the intervention at their own expense after recruitment for the study is completed
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Source(s) of Monetary Support
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European Union's Horizon 2020 Framework Programme for Research and Innovation
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Ethics review
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Status:
Approval date:
Contact:
TU Dresden Ethics Committee, 23/02/2016, ref: EK83032016
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Results
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Results available:
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Yes |
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Date Posted:
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Date Completed:
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15/06/2019 |
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URL:
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