Frequency of Hypermobility-Related Problems in Patients With Anorexia Nervosa
1 other identifier
observational
100
1 country
1
Brief Summary
The purpose of this study is to examine the frequense of generalized hypermobility and pain in patients with Anorexia Nervosa. The study further explores two main questions: (1) whether generalized hypermobility may be an explanatory factor for pain in some patients with Anorexia Nervosa, and (2) whether temporomandibular joint problems (such as instability, pain, difficulties opening the mouth, locking, or clicking) contribute to eating difficulties in certain individuals with Anorexia Nervosa.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 21, 2025
CompletedFirst Posted
Study publicly available on registry
September 8, 2025
CompletedStudy Start
First participant enrolled
September 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 30, 2026
September 8, 2025
August 1, 2025
11 months
August 21, 2025
August 28, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Joint hypermobility
Joint mobility will be assessed according to the Beighton score using a goniometer.
One-time assessment at baseline (Day 0, at the inclusion visit).
5-part questionnaire
Participants over the age of 18 will also complete the 5-part questionnaire regarding historical hypermobility.
One-time questionnaire at baseline (Day 0, after clinical examination).
Secondary Outcomes (3)
Joint pain
One-time questionnaire at baseline (Day 0, after clinical examination).
Temporomandibular joint problems
One-time questionnaire at baseline (Day 0, after clinical examination).
Pain drawing
One-time questionnaire at baseline (Day 0, after clinical examination).
Study Arms (1)
Female patients diagnosed with Anorexia Nervosa or Atypical Anorexia Nervosa, aged 13-25 years.
Eligibility Criteria
Patients at the Eating Disorders Center for Children and Young Adults in Gothenburg.
You may qualify if:
- Female patients Aged 13-25 years
- Diagnosed with:
- Anorexia Nervosa (ICD-10 F50.0), or
- Atypical Anorexia Nervosa (ICD-10 F50.1)
- Currently receiving treatment or scheduled to receive treatment
You may not qualify if:
- Severe cognitive impairment
- Insufficient Swedish language skills that make it impossible to provide informed consent and prevent answering study questions
- Pregnancy and up to one year postpartum
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Queen Silvias Children´s Hospital
Gothenburg, Västra Götaland County, 416 50, Sweden
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr
Study Record Dates
First Submitted
August 21, 2025
First Posted
September 8, 2025
Study Start
September 15, 2025
Primary Completion (Estimated)
July 30, 2026
Study Completion (Estimated)
July 30, 2026
Last Updated
September 8, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share