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Clinical Trial Summary

We will evaluate the acceptability and feasibility of a 8-week long digital mindfulness-based intervention for anorexia nervosa and bulimia nervosa. This study is a prospective single-arm trial during the intervention development phase. Following this phase, after the intervention has been further developed, a subsequent study (with a different clinicaltrials.gov identification #) will utilize a randomized control trial design.


Clinical Trial Description

Procedures include completing: (1) pre-intervention screening assessment; (2) brief daily assessments for the first and last weeks of the study (4 times per day); (3) an initial baseline visit; (4) 8-week web-based intervention (3) a post-intervention assessment (8-weeks after baseline); and (4) a brief 8-week follow-up assessment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05753410
Study type Interventional
Source Yeshiva University
Contact
Status Recruiting
Phase N/A
Start date March 1, 2023
Completion date March 1, 2024

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