Health-Related Quality of Life in Patients With Dupuytren's Disease

Hamilton Health Sciences (HHS)

Status: Completed

Conditions: Dupuytren's Contracture

Study type: Observational

Funder types: Other

Identifiers

NCT00468949

06-2713

Details and patient eligibility

About

Main Research Questions:

We want to measure the change in quality of life in Dupuytren's disease patients who do and do not undergo surgery. Also, we want to test the validity of health related quality of life measurements in patients with Dupuytren's disease.

Why is this research important? Some patients with Dupuytren's contracture require excision surgery or palmar fasciectomy. Other patient's with Dupuytren's contracture do not require surgery; however, these patients may need surgery in the future. No studies have reported the health-related quality of life of patients with Dupuytren's disease whether related to surgical intervention or not.

What is being studied? We are studying the difference and change in health-related quality of life in patients suffering from Dupuytren's disease who require excision surgery and do not require surgery.

Full description

Previous research on Dupuytren's disease has not reported the health-related quality of life (HRQL) of patients' whether related to surgical intervention or not. The primary objective of this study is to measure the change in HRQL in Dupuytren's contracture patients who do and do not undergo palmar fasciectomy. Health related quality of life will be measured using the 1) Health Utilities Index Mark III (HUI3); 2) Short Form-36 (SF-36); and the 3) Michigan Hand Outcomes Questionnaire (MHQ). The secondary objective is to look at the measurement properties, including the reliability and responsiveness, of each of the three HRQL instruments when they are used in patients with Dupuytren's contracture. We will also assess the concurrent validity of each of the HRQL instruments.

Enrollment: 51 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• patients who have the diagnosis of Dupuytren's disease
• able to comprehend English to complete the self-reported questionnaires
• willing to provide informed consent.

Exclusion criteria

• patients who have had previous Dupuytren's contracture surgery on the same hand
• patients who have carpal tunnel syndrome, rheumatoid arthritis, connective tissue disorder, tenosynovitis, or another condition that could affect quality of life
• patients who are under the age of 18 years.

Trial design

51 participants in 2 patient groups

1

Description:

Patients undergoing excision surgery for their dupuytren's contracture

2

Description:

Patients not undergoing surgery for their excision surgery