Chronic Pain Clinical Trial
Official title:
Guided Internet-delivered Cognitive-behavioral Therapy for Former Chronic Pain Patients: Randomised Controlled Trial
| NCT number | NCT01491269 |
| Other study ID # | smartaMB2011 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | August 2009 |
| Est. completion date | June 2010 |
| Verified date | December 2023 |
| Source | Linkoeping University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The aim of the present study was to investigate if guided Internet-delivered Cognitive-behavioral Therapy (CBT) would help chronic pain patients who had previously undergone a multidisciplinary treatment but still have residual problems.
| Status | Completed |
| Enrollment | 72 |
| Est. completion date | June 2010 |
| Est. primary completion date | December 2009 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility | Inclusion Criteria: - to have been medically investigated (within one year) - completed the multidisciplinary rehabilitation program - have residual symptoms after the rehabilitation treatment (defined as functional impairment caused by their pain) - have Internet access Exclusion Criteria: - planned surgery - ongoing medical investigation that could impede participation in the study - suffering from acute physical or psychological conditions - people confined to wheelchairs - people not fluent with the Swedish language |
| Country | Name | City | State |
|---|---|---|---|
| Sweden | Uppsala University | Uppsala |
| Lead Sponsor | Collaborator |
|---|---|
| Gerhard Andersson |
Sweden,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | The Coping Strategies Questionnaire (CSQ) | The CSQ contains 50 items divided in eight scales that measures different cognitive and behavioral coping strategies. The different coping strategies are: diverting attention, re-interpreting pain sensations, coping self-statements, ignoring sensations, praying and hoping, catastrophizing, increased behavioral activities and pain behavior (Rosenthiel & Keefe, 1983). Change from baseline in the different subscales pre- and post treatment. | One week pre treatment, one week post treatment | |
| Secondary | Hospital Anxiety and Depression Scale, HADS | HADS is a 14-item questionnaire, and is designed to measure anxiety and depression in non-psychiatric patients. | One week pre treatment, one week post treatment | |
| Secondary | Multidimensional Pain Inventory, MPI | MPI, assess psychosocial and behavioural consequences of pain. It´s divided into 2 sections and consisting of 8 scales. These are: Pain Severity, Interference, Life Control, Affective Distress, Support, Punishing Responses, Solicitous Responses and Distracting Responses. | One week pre treatment, one week post treatment | |
| Secondary | Pain and Impairment Relationship Scale (PAIRS) | PAIRS consist of 15 personal statements that reflect thoughts, attitudes and opinions about pain. The questionnaire assesses beliefs and attitudes that patients have regarding pain and ability to function despite discomfort. | One week pre treatment, one week post treatment | |
| Secondary | Quality of Life Inventory (QOLI) | QOLI contains 32 items for assessing life satisfaction. The assessment yields an overall score and profile in 16 areas of life; health, self-esteem, goals and values, money, work, play, learning, creativity, helping, love, friends, children, relatives, home, neighborhood and community. Each item is rated in terms of importance and satisfaction. | One week pre treatment, one week post after treatment | |
| Secondary | Chronic Pain Acceptance Questionnaire (CPAQ) | CPAQ contains 20 items divided in two scales, engagement and willingness. CPAQ measures acceptance in relation to chronic pain. | One week pre treatment, one week post treatment |
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