Health-Related Quality of Life in Patients With Dupuytren's Disease
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Purpose
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.
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Health-Related Quality of Life in Patients With Dupuytren's Disease: A Prospective Cohort Study. |
| Enrollment: | 51 |
| Study Start Date: | May 2007 |
| Study Completion Date: | July 2011 |
| Primary Completion Date: | July 2011 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
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1
Patients undergoing excision surgery for their dupuytren's contracture
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2
Patients not undergoing surgery for their excision surgery
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Detailed 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.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Patients with dupuytren's contracture
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.
Contacts and Locations| Canada, Ontario | |
| St. Joseph's Healthcare | |
| Hamilton, Ontario, Canada, L8N 4A6 | |
| Principal Investigator: | Achilleas Thoma, MD MSC | St. Josephs Hamilton Health Care / McMaster University |
More Information
No publications provided
| Responsible Party: | Dr. Achilleas Thoma, McMaster University |
| ClinicalTrials.gov Identifier: | NCT00468949 History of Changes |
| Other Study ID Numbers: | 06-2713 |
| Study First Received: | May 2, 2007 |
| Last Updated: | July 27, 2011 |
| Health Authority: | Canada: Ethics Review Committee |
Keywords provided by McMaster University:
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Health-Related Quality of Life Dupuytren's Disease Health Utilities Index Short Form-36; Michigan Hand Outcomes Questionnaire |
Additional relevant MeSH terms:
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Contracture Dupuytren Contracture Joint Diseases |
Musculoskeletal Diseases Muscular Diseases Connective Tissue Diseases |
ClinicalTrials.gov processed this record on June 18, 2013