Returning to Work. Efficacy of "Tailored Physical Activity or" "Chronic Pain Self-management Program" in Sicklisted Citizens With Chronic Musculoskeletal Pain
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
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
| Condition | Intervention | Phase |
|---|---|---|
|
Musculoskeletal Pain |
Other: Tailored Physical Activity Behavioral: "Chronic Pain Self-management Programme" Behavioral: Health counselling |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Efficacy of "Tailored Physical Activity or" "Chronic Pain Self-management Program" on Returning to Work: a Randomized Controlled Trial in Sicklisted Citizens With Chronic Pain Related to the Spine or Upper Body |
- Sick-listed or not [ Time Frame: 3 months ] [ Designated as safety issue: No ]Registration of the participants status as sick-listed or not and co-primary the number of days on sick-leave in the period.
- Aerobic capacity [ Time Frame: 3 months ] [ Designated as safety issue: No ]
- hand-grip strength [ Time Frame: 3 months ] [ Designated as safety issue: No ]
- Body weight, waist circumference, hip circumference [ Time Frame: 3 months ] [ Designated as safety issue: No ]
- Questionnaire [ Time Frame: 3 months ] [ Designated as safety issue: No ]
- Sick-listed or not [ Time Frame: 12-months follow-up ] [ Designated as safety issue: No ]Registration of the participants status as sick-listed or not and co-primary the number of days on sick-leave in the period.
- Aerobic capacity [ Time Frame: 12-months follow-up ] [ Designated as safety issue: No ]
- Hand-grip strength [ Time Frame: 12-months follow-up ] [ Designated as safety issue: No ]
- Questionnaire [ Time Frame: 12-months follow-up ] [ Designated as safety issue: No ]
- Body weight, waist circumference, hip circumference [ Time Frame: 12 months follow-up ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 138 |
| Study Start Date: | May 2011 |
| Estimated Study Completion Date: | July 2013 |
| Estimated Primary Completion Date: | July 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Tailored Physical Activity |
Other: Tailored Physical Activity
Health counselling (1,5h) and graded physical activity (3×50 min/week in 10 weeks)
|
| Active Comparator: "Chronic Pain Self-management Programme" |
Behavioral: "Chronic Pain Self-management Programme"
Health counselling (1,5h) and 'Chronic Pain Self-management Program' (2,5h in 6 weeks)
|
| Health Counselling |
Behavioral: Health counselling
Health guidance (1,5h)
|
Detailed 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.
Eligibility| Ages Eligible for Study: | 18 Years to 66 Years |
| Genders Eligible for Study: | Both |
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
Contacts and Locations| Contact: Karen Søgaard, Professor, ph.d. | 004565504409 | ksogaard@health.sdu.dk |
| Contact: Lotte Nygaard Andersen, cand.scient. | 004524407841 | lonygaard@health.sdu.dk |
| Denmark | |
| Health Care Centre | Recruiting |
| Sønderborg, Denmark, 6400 | |
| Contact: Lene Gram Herborg 004588725192 lghe@sonderborg.dk | |
More Information
Additional Information:
No publications provided by University of Southern Denmark
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Lotte Nygaard Andersen, Ph.d. fellow, University of Southern Denmark |
| ClinicalTrials.gov Identifier: | NCT01356784 History of Changes |
| Other Study ID Numbers: | 95-154-32028 |
| Study First Received: | May 13, 2011 |
| Last Updated: | April 19, 2013 |
| Health Authority: | Denmark: Danish Dataprotection Agency |
Keywords provided by University of Southern Denmark:
|
Sick-listed Tailored physical activity Patient education Returning to work |
DK-Sønderborg Municipality columna upper body |
ClinicalTrials.gov processed this record on May 19, 2013