NCT07159867

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

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
3mo left

Started Sep 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress74%
Sep 2025Jul 2026

First Submitted

Initial submission to the registry

August 21, 2025

Completed
18 days until next milestone

First Posted

Study publicly available on registry

September 8, 2025

Completed
7 days until next milestone

Study Start

First participant enrolled

September 15, 2025

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2026

Last Updated

September 8, 2025

Status Verified

August 1, 2025

Enrollment Period

11 months

First QC Date

August 21, 2025

Last Update Submit

August 28, 2025

Conditions

Keywords

Anorexia nervosaJoint hypermobilityPainTemporomandibular joint

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

Age13 Years - 25 Years
Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

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

Location

MeSH Terms

Conditions

Anorexia NervosaJoint InstabilityPain

Condition Hierarchy (Ancestors)

Feeding and Eating DisordersMental DisordersJoint DiseasesMusculoskeletal DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Elke Schubert Hjalmarsson, PhD

CONTACT

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

Locations