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Musculoskeletal pain in adolescents with Generalized Joint Hypermobility in the context of activity impairment

Musculoskeletal pain in adolescents with Generalized Joint Hypermobility in the context of activity impairment - Musculoskeletal pain and Generalized Joint Hypermobility

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON46951
Enrollment
75
Registered
2018-06-20
Start date
2016-03-09
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Ehlers-Danlos (hypermobility type) Hypermobility Syndrome

Interventions

Gait analysis
Generalized joint hypermobility
Hypermobility Syndrome
Musculoskeletal pain

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
12 Years to 64 Years

Inclusion criteria

Inclusion criteria: Inclusion will be based on one of the following diagnoses:;Hypermobility Syndrome: according to the Brighton criteria Ehlers Danlos (hypermobility type): Villefranche criteria Generalized Joint Hypermobility: Beighton score >4

Exclusion criteria

Exclusion criteria: Primary exclusion criteria encompass the presence of other heritable disorders of connective tissue (HDCT) like Ehlers-Danlos (other than the hypermobile type), Marfan syndrome or osteogenesis imperfecta. If genetic screening rules out HDCT*s, the participant is again eligible for inclusion in the study.;Secondary exclusion criteria encompass: -A history of surgery is present on the extremities, spine or thorax that could interfere with walking, or with arm/hand function related activities. -Any conditions that render the participant too unfit to be tested (such as pulmonary and/or cardiac disorders) -Any conditions that render the participant unable to understand or adhere to the protocol (such as cognitive, social, visual and/or language problems, or hand problems, that render the patient unfit to fill-in the questionnaires).

Design outcomes

Primary

MeasureTime frame
The primary outcomes will be set at the amount of activity impairment.

Secondary

MeasureTime frame
Secondary outcomes will entail potential contributing factors for activity impairment in terms of Musculoskeletal complaints (pain and fatigue), physical factors (Joint biomechanics, muscle power, proprioception) and psychological factors (psychological comorbidity and parental factors).

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)