ID
Bron
Verkorte titel
Aandoening
Specific and non-specific CANS, complaints of the arm, Upper Extremity, Hand, Disability Evaluation, Investigative Techniques, CANS, Bovenste extremiteit, Hand, Beoordelen van beperkingen, Onderzoekstechnieken
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Each part (I, II and III) of the study has its own main study parameters.<br>
Part I. Scores of single items, subscales and a total score of three questionnaires (QuickDASH, PRWHE, HFS).<br>
Part II. Scores of eight different tests composing the upper extremity FCE.<br>
Part III. Maximal oxygen uptake (VO2max in l/min).
Onderzoeksopzet
Part I: T1 (first measurement), T2 (1-3 weeks after T1), T3 (4-8 weeks after start of hand therapy, where applicable).
Part II: T1 (first measurement), T2 (1-3 weeks after T1), T3 (4-8 weeks after start of hand therapy, where applicable).
Part III: T1 (first measurement).
Onderzoeksproduct en/of interventie
N/A
Publiek
R.J. Berduszek
PO BOX 30.001
Groningen 9700 RB
The Netherlands
+31503612295
r.j.berduszek@umcg.nl
Wetenschappelijk
R.J. Berduszek
PO BOX 30.001
Groningen 9700 RB
The Netherlands
+31503612295
r.j.berduszek@umcg.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
In order to be eligible to participate in this study (part I, II and III), a subject must meet all of the following criteria:
- Aged 18 years or over.
- Complaints of hand, wrist and/or forearm, classified as either specific or nonspecific complaints of the arm, neck and/or shoulder (CANS), which might have a direct influence on hand or wrist function (in practice all complaints located from the elbow towards the fingers).
Extra for assessing responsiveness in part I:
- Receiving hand therapy for these complaints at the outpatient clinic of the Department of Rehabilitation Medicine of the University Medical Center Groningen, for a duration of at least four weeks.
Extra for the functional capacity evaluation study (part II):
- Meeting the criteria of the Physical Activity Readiness Questionnaire (PAR-Q). If question 5 (‘Do you have a bone or joint problem that could be made worse by a change in your physical activity’) is solely answered with ‘yes’ because of those complaints of hand, wrist and/or forearm for which the patient visited the outpatient clinic of the Department of Rehabilitation Medicine of the University Medical Center Groningen, we consider the criteria of the PAR-Q are still being met.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
A potential subject who meets any of the following criteria will be excluded from participation in this study (parts I, II and III):
- Insufficient understanding of Dutch to fill out questionnaires.
- Other medical condition(s) causing considerate disability, such as neurological disorders (e.g. stroke, peripheral nerve damage) or joint diseases (e.g. osteoarthritis, rheumatoid arthritis).
Extra for part III:
- Presence of contraindications for cardiopulmonary exercise testing. This is checked using usual clinical criteria, based on the ATS/ACCP Statement on cardiopulmonary exercise testing.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL5657 |
NTR-old | NTR5792 |
CCMO | NL51584.042.15 |
OMON | NL-OMON41867 |