Actively Recruiting
Mealtime Anxiety in Eating Disorders
Led by Oslo University Hospital · Updated on 2025-06-27
40
Participants Needed
1
Research Sites
116 weeks
Total Duration
On this page
Sponsors
O
Oslo University Hospital
Lead Sponsor
T
The Dam Foundation
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this observational study is to assess mealtime anxiety in patients with eating disorders receiving treatment at an in-patient unit. Anxiety wil be assessed using ecological momentary assessment (EMA). The main research question is: • Does post meal activity reduce anxiety in patients with eating disorders? Study participation will last for two weeks. Participants will be reporting current levels of anxiety/distress on an EMA mobile app during treatment as usual. During one of the two study participation weeks, the participants will perform post mealtime activity.
CONDITIONS
Official Title
Mealtime Anxiety in Eating Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All patients admitted to the Regional Department for Eating Disorders adult in-patient unit (over 16 years old) will be invited to participate.
You will not qualify if you...
- Patients who receive tube feeding for all meals during the study period will be excluded.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Oslo University Hospital, Regional Department for Eating Disorders
Oslo, Norway
Actively Recruiting
Research Team
K
Kristin Stedal, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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