Pain Clinical Trial
Official title:
Development, Evaluation and Cost Effectiveness of a Treatment Program With a Behavioural Medicine Approach for Adolescents With Persistent Pain.
| NCT number | NCT01381263 |
| Other study ID # | Dnr 2010/047 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | January 2011 |
| Est. completion date | December 2013 |
| Verified date | May 2018 |
| Source | Uppsala University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Recurrent pain, such as headache, stomach pain and musculoskeletal pain is common in children
and adolescents. Children and adolescents are reported to have restrictions in daily life
activities, social contacts, and school attendance, and to have poorer academic skills and as
well as an increased utilization of heath care services due to pain problems. The treatment
approaches available today for teenagers with pain are often biological/physiological and
little evidence for their effectiveness has been shown. It is urgent to try new interventions
for pain problems in early ages in order to prevent disability, development of maladaptive
coping strategies and to avoid negative impact on daily activities.
The optimal treatment regime for paediatric pain patients has been suggested to be cognitive
behavioural approach integrated with physical therapy The aim of this project is to develop
and evaluate in a randomized controlled trial a treatment program with a behavioural medicine
approach (suitable to use in primary care or school based health care context) compared with
standard treatment for adolescents with persistent pain problems. The aim is also to compare
short and long-term costs for patients and for the health care system related to the two
interventions, in order to determine strategies for future cost-effective care of children
and adolescents experiencing recurrent pain.
| Status | Completed |
| Enrollment | 100 |
| Est. completion date | December 2013 |
| Est. primary completion date | December 2013 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 12 Years to 16 Years |
| Eligibility |
Inclusion Criteria: - Adolescents with pain and interference of daily activities due to pain, referred to paediatric physiotherapy in a primary health setting will be included. - Participants must understand written and oral Swedish and have had persistent pain for more than 6 weeks or recurrent pain more than once a week for over three months. - The adolescents´ parents will be included in a brief intervention. Exclusion Criteria: - Subjects with resent trauma, ongoing treatment for any psychiatric illness or cognitive problems will be excluded. |
| Country | Name | City | State |
|---|---|---|---|
| Sweden | Samariterhemmet | Uppsala |
| Lead Sponsor | Collaborator |
|---|---|
| Uppsala University | The Swedish Research Council, Uppsala County Council, Sweden |
Sweden,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in Functional Disability Inventory | Functional Disability Inventory assesses children's self reported difficulties in physical and psychosocial functioning due to the child's physical health. FDI consists of 15 items describing limitations of activities during the past two weeks. Each item is scored on a 5-point (0-4) where a higher score indicates greater disability. The FDI has been reported to have a high validity and reliability and can be used for children and adolescents with recurrent and chronic pain. | 6 months, one year and 2 years post treatment |
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