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Investigation of Psychometric Properties of the EuroQoL EQ-5D-5L in Patients With Carpal Tunnel Syndrome

Investigation of Psychometric Properties of the EuroQoL EQ-5D-5L in Patients With Carpal Tunnel Syndrome

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02276105
Enrollment
60
Registered
2014-10-27
Start date
2014-10-31
Completion date
2015-05-31
Last updated
2015-05-21

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

Conditions

Carpal Tunnel Syndrome

Keywords

Carpal Tunnel Syndrome, Quality of Life, EQ-5D, SF-12, Michigan Hand Questionnaire

Brief summary

The purpose of this study is to determine how appropriate and practically is the EQ-5D questionnaire in use on patients with carpal tunnel syndrome undergoing surgery along the change of quality of life.

Detailed description

Carpal Tunnel Syndrome (CTS) is one of the most indications in hand surgery. To rate surgery's outcome, hand-specific instruments like the Michigan Hand Questionnaire (MHQ) are used as well as questionnaires which refers to the quality of life (QOL). In clinical daily grind, the SF-12 or the EQ-5D are common instruments to gain information about the patient's QOL. At the time, there is no current evidence available while using standardized questionnaires like the EQ-5D to capture the change in QOL in patients with CTS undergoing surgery. It would be interesting to assert that the investigation offers results about the patient's QOL and its change. Therefore, the aim of the study is to investigate the psychometric properties of the EQ-5D on patients with CTS undergoing surgery.

Interventions

OTHERQuestionnaires

On three time-points (Baseline, Retest, Follow-Up), each participant has to fill out the questionnaires: Michigan Hand Questionnaire, EuroQol EQ-5D-5L and the Short Form SF-12 Health Survey

Sponsors

Schulthess Klinik
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age over 18 years * diagnosed CTS * planned surgical decompression of the carpal tunnel * signed informed consent

Exclusion criteria

* additional simultaneously performed hand surgery of the affected limb * recurrent surgery on the already involved hand * the other hand is already included in the study * disease, which do not allow appropriated analysis of data like central-neurological, psychiatric or metabolic disease * legal incompetence

Design outcomes

Primary

MeasureTime frame
Quality of life measured with the EQ5Dfrom two weeks before surgery (Baseline) to six weeks postoperative (Follow-Up)

Secondary

MeasureTime frame
Hand function measured with the MHQfrom two weeks before surgery (Baseline) to six weeks postoperative (Follow-Up)
Quality of life measured with the SF 12from two weeks before surgery (Baseline) to six weeks postoperative (Follow-Up)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026