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| Name | Class |
|---|---|
| Finnish Work Environment Fund | OTHER |
| Työterveys Helsinki (Helsinki city occupational health service) | UNKNOWN |
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This cluster randomized waiting-list controlled study will evaluate the effectiveness of pain management group activity organized by the OH on pain intensity and associated disability, and co-occurrence of mental or sleep problem in patients with chronic pain.
Pain is very prevalent among the working population causing a considerable amount of work disability days. Pain management group therapy has shown to have a significant effect on chronic pain. However, little is known of the effect of such therapy on work disability. There are especially very few studies prescribing the effectiveness of pain management groups provided by the occupational health service.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Pain management group | Experimental | 6 + 1 meetings 2 hours each |
|
| Treatment as usual | No Intervention | Waiting list - will receive treatment as usual |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Pain management group | Behavioral | Chronic pain patients participate in a peer group. They are provided information about chronic pain self-management based on biopsychosocial framework. |
| Measure | Description | Time Frame |
|---|---|---|
| Pain intensity | self-reported questionnaire, 1-item question, scale 0-10, n=60 | Change in pain intensity from before intervention to immediately after intervention and at 6 months |
| Pain self-efficacy | self-reported questionnaire, set of 10 questions, item response scale 0 - 6, n=60 | Change in pain self-efficacy from before intervention to immediately after intervention and at 6 months |
| Chronic pain acceptance | self-reported questionnaire, set of 8 questions, item response scale 0 - 6, n=60 | Change in chronic pain acceptance from before intervention to immediately after intervention and at 6 months |
| Fear-avoidance beliefs | self-reported questionnaire, set of 3 questions, item response scale 0 - 6, n=18 | Change in fear-avoidance beliefs from before intervention to immediately after intervention and at 6 months |
| Depressive symptoms | self-reported questionnaire, 1-item question, response scale 0-10, n=60 | Change in depressive symptoms from before intervention to immediately after intervention and at 6 months |
| Sleep problems | self-reported questionnaire, 1-item question, response scale 0-10, n=60 | Change in sleep problems from before intervention to immediately after intervention and at 6 months |
| Work ability |
| Measure | Description | Time Frame |
|---|---|---|
| sickness absence | register based, number of sick leave days | 6 months before and 6 months after intervention |
| health care contacts | register based, number of contacts to OHS |
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Inclusion Criteria:
- chronic pain + increased risk of work disability (based on a screening survey)
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Helena Miranda, Dr.Med.Sc. | Helsinki City OHS | Principal Investigator |
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| ID | Term |
|---|---|
| D059350 | Chronic Pain |
| D000377 | Agnosia |
| ID | Term |
|---|---|
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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self-reported questionnaire, 1-item question, response scale 0-10, n=60
| Change in work ability from before intervention to immediately after intervention and at 6 months |
| 6 months before and 6 months after intervention |
| D010468 | Perceptual Disorders |
| D019954 | Neurobehavioral Manifestations |
| D009422 | Nervous System Diseases |