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Clinical Trials/NCT00902863
NCT00902863
Terminated
Not Applicable

The Impact of a Course on Stress Reduction Techniques on Satisfaction, Stress, Performance, and Quality of Life in Patients With Chronic Pain

Hamilton Health Sciences Corporation1 site in 1 country5 target enrollmentFebruary 2009
ConditionsChronic Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Pain
Sponsor
Hamilton Health Sciences Corporation
Enrollment
5
Locations
1
Primary Endpoint
Performance and Satisfaction using Canadian Occupational Performance Measure (COPM)
Status
Terminated
Last Updated
15 years ago

Overview

Brief Summary

This project seeks to measure the effectiveness of a course in self-management strategies (including yoga, mindfulness, and breathing exercises). The course will be provided by a certified yoga instructor to patients being followed at the Pain Management Centre, Hamilton Health Sciences (HHS).

Detailed Description

The Pain Management Centre at Hamilton Health Sciences is organizing a course in stress reduction techniques for patients with chronic pain. The Pain Centre has arranged for a local certified yoga instructor to lead a 6-week course that she has developed for our specific patient population. The course will include self-management strategies for pain control, such as breathing exercises, yoga poses, and mindfulness meditation. Standardized questionnaires and a semi-structured interview to record baseline and post-course outcomes. The study will involve the following questionnaires/surveys/interviews: 1) Canadian Occupational Performance Measure, 2) Perceived Stress Scale, 3) Burckhardt Quality of Life Scale, 4) Visual Analog Score, and 5) written questions concerning patient demographics, the patient's chronic pain condition, and their satisfaction with the course. The participants would be asked to fill out questionnaires at three different times: 1) baseline data collected within two weeks of starting course, 2) short-term outcome data within two weeks of completing course, and 3) long-term outcome data four to six months after the course.

Registry
clinicaltrials.gov
Start Date
February 2009
End Date
March 2010
Last Updated
15 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • patients have a history of moderate to severe chronic pain

Exclusion Criteria

  • non-English speaking patients

Outcomes

Primary Outcomes

Performance and Satisfaction using Canadian Occupational Performance Measure (COPM)

Time Frame: 6 months

Secondary Outcomes

  • Pain relief using VAS and pain scores(6 months)

Study Sites (1)

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