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Reliability of the FCE-OH, and its relation with musculoskeletal complaints.

Reliability of the FCE-OH, and its relation with musculoskeletal complaints.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON29561
Enrollment
50
Registered
2016-03-01
Start date
2016-03-06
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

Upper limb amputation, functional capacity evaluation, physical capacity, musculoskeletal complaints.

Interventions

Patients perfrom a functional capacity evaluation test twice, with approximately two/three days in between. Furthermore patients answer a questionnaire on musculoskeletal complaints and one on pain re

Sponsors

No sponsors.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - 18-62 years of age - Transversal reduction deficiency or ampupation of the upper limb at or proximal to the level of the wrist - Normal hand function of the unaffected hand

Exclusion criteria

Exclusion criteria: - Invalidating or serious pulmonary or cardiac health problems - Balance problems

Design outcomes

Primary

MeasureTime frame
- FCE-tests results (Each test is analysed separately, no total score is computed) - Outcomes of the compensatory movement scale (per item, and one total score) - Presence of MSC during the previous four weeks and last year - Occurrence of pain response and serious adverse events

Secondary

MeasureTime frame
- Borg CR10 scale outcomes - Difference in heart rate measured before and after each test or trial (computed as [heart rate after test/trial divided by heart rate before test/trial multiplied by 100%)] - Gender, age, and work status - Prosthesis use (yes/no, type of prosthesis, and years of experience with a prosthesis) - General health (subscale of the SF-36)

Contacts

Public ContactSietke G. Postema

Medical Center Groningen, Department of Rehabilitation Medicine

S.G.Postema@umcg.nl0031 3618041

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)