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Targeted prevention for women with subclinical anorexia nervosa - Student Bodies-AN (SB-AN)

Targeted prevention for women with subclinical anorexia nervosa - Student Bodies-AN (SB-AN): a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN70380261
Enrollment
168
Registered
2014-04-22
Start date
2012-11-15
Completion date
Unknown
Last updated
2022-06-20

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

Conditions

Women with subclinical anorexia nervosa and/or at risk for the development of anorexia nervosa Mental and Behavioural Disorders Anorexia nervosa

Interventions

Eligible women (aged 18 and above) will be screened at universities in different cities in Germany (planned cities: Dresden, Halle, Leipzig, Berlin, Hamburg) and two higher-risk environments. Followin

Sponsors

Else Kröner-Fresenius Foundation (Germany)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Age = 18 years 2. Informed consent 3. Female gender 4. High weight and shape concerns (WCS > 42) 5. 17.5 = BMI = 21 OR 21 < BMI = 25 AND restrictive eating (EDE-Q Restraint = 2.6; = more than 1 SD above the mean of healthy controls)

Exclusion criteria

Exclusion criteria: 1. Current full-syndrome (DSM-IV) anorexia nervosa, bulimia nervosa or binge eating disorder 2. Serious medical or mental problems that would prohibit participation in the trial, i.e. current substance abuse, acute or chronic organic or schizophrenic psychosis 3. Severe suicidal ideation or behavior 4. No Internet access

Design outcomes

Primary

MeasureTime frame
1. The rates (%) of participants with a decrease in the Eating Disorder Examination (EDE) total score below a score of 1.87 between pre-intervention and 12-month follow-up 2. The rates (%) of underweight participants with a BMI increase of at least 0.8 kg/m² between pre-intervention and 12-month follow-up

Secondary

MeasureTime frame
The following outcomes will be measured at baseline, after the last session of SB-AN (10 weeks), six months after the program was finished and 12 months after the program was finished: 1. Eating Disorder Examination subscales (EDE-Weight Concern, EDE-Shape Concern, EDE-Eating Concern, EDE-Restraint) 2. Number of binges (for binge eating subgroup) 3. Frequency of participants fulfilling criteria for EDNOS The following outcomes will be measured at baseline, after the fifth session of SB-AN, after the last session of SB-AN (10 weeks), six months after the program was finished, 12 months after the program was finished: 1. Weight Concern Scale (WCS) 2. Eating Disorder Inventory-2 (EDI-2), subscales: Drive for Thinness, Bulimia, Body Dissatisfaction 3. Beck Depression Inventory-II (BDI-II) 4. Brief Symptom Inventory (BSI) 5. Exercise Dependence Questionnaire (EDQ) 6. Frost Multidimensional Perfectionism Scale (FMPS) 7. Clinical Impairment Assessment (CIA) 8. Knowledge test

Countries

Germany

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 13, 2026