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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01356784
Other study ID # 95-154-32028
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received May 13, 2011
Last updated April 22, 2014
Start date May 2011
Est. completion date April 2014

Study information

Verified date April 2014
Source University of Southern Denmark
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Dataprotection Agency
Study type Interventional

Clinical Trial Summary

TEst the effect of "Tailored Physical Activity" or "Chronic Pain Self-management Program" on Returning to Work in Sicklisted Citizens With Chronic Pain Related to the Spine or Upper Body


Description:

Pain affects quality of life and it's important for the individual who experience chronic pain to find strategies to prevent or reduce pain. In some situations pain can't be reduced and the individual has to master pain by learning to live with it. Pain can lead to a loss of functions which may change one's roles both in relation to the family as to colleagues, for example sick leave from work.

Limited evidence is available on the effects of interventions to sick-listed citizens with chronic musculoskeletal pain.

This study test the effect of either "tailored physical activity or "Chronic Pain Self-management Program" on returning to work and the parameters pain, function and quality of life respectively on the body function and participation level of sick-listed people with chronic musculoskeletal pain related to columna and the upper body.

Citizens in DK-Sønderborg Municipality sick-listed for a maximum of 9 weeks will be invited. Participants will be randomized for either tailored physical activity, "Chronic Pain Self-Management Program" or reference group.

Primary endpoint is 3 months and 12 months follow-up.


Recruitment information / eligibility

Status Completed
Enrollment 141
Est. completion date April 2014
Est. primary completion date July 2013
Accepts healthy volunteers
Gender Both
Age group 18 Years to 66 Years
Eligibility Inclusion Criteria:

- Sick-listed with musculoskeletal pain related to columna or the upper body for a maximum period of 9 weeks in DK-Sønderborg Municipality

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Tailored Physical Activity
Health counselling (1,5h) and graded physical activity (3×50 min/week in 10 weeks)
Behavioral:
"Chronic Pain Self-management Programme"
Health counselling (1,5h) and 'Chronic Pain Self-management Program' (2,5h in 6 weeks)
Health counselling
Health guidance (1,5h)

Locations

Country Name City State
Denmark Health Care Centre Sønderborg

Sponsors (2)

Lead Sponsor Collaborator
University of Southern Denmark DK-Sønderborg Municipality

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sick-listed or not Registration of the participants status as sick-listed or not and co-primary the number of days on sick-leave in the period. 3 months No
Secondary Aerobic capacity 3 months No
Secondary hand-grip strength 3 months No
Secondary Body weight, waist circumference, hip circumference 3 months No
Secondary Questionnaire 3 months No
Secondary Sick-listed or not Registration of the participants status as sick-listed or not and co-primary the number of days on sick-leave in the period. 12-months follow-up No
Secondary Aerobic capacity 12-months follow-up No
Secondary Hand-grip strength 12-months follow-up No
Secondary Questionnaire 12-months follow-up No
Secondary Body weight, waist circumference, hip circumference 12 months follow-up No
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