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Multidisciplinary behavioural program for coping with chronic neuropathic pain following spinal cord injury.

Multidisciplinary behavioural program for coping with chronic neuropathic pain following spinal cord injury. - Behavioural program for neuropathic pain following SCI.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON32405
Enrollment
80
Registered
2008-08-19
Start date
2009-02-26
Completion date
Unknown
Last updated
2024-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

nerve pain neuropathic pain

Interventions

The multidisciplinary program, comprising educational, cognitive, and behavioural interventions in the treatment of coping with chronic neuropathic pain, consists of ten sessions of 3 hours over a 1

Sponsors

Revalidatiecentrum De Hoogstraat
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: (1) spinal cord injury; (2) at least 18 years old; (3) at least one year and at most five years after discharge from first inpatient spinal cord injury rehabilitation; (4) main type of pain is severe chronic neuropathic pain.

Exclusion criteria

Exclusion criteria: (1) spinal cord injury by a malignant tumor; (2) former cognitive behavioural therapy for coping with pain after spinal cord injury; (3) inability to function in a group by major language problems or psychopathology; (4) insufficient mastery of the Dutch language.

Design outcomes

Primary

MeasureTime frame
Pain severity and impact of pain: Chronic Pain Grade questionnaire.

Secondary

MeasureTime frame
- Level of activation and participation: Utrecht Activities List, - Life satisfaction: Life Satisfaction Questionnaire, and - Mood: Hospital Anxiety and Depression Scale. Demographic (e.g., age and gender), disease and pain characteristics (e.g., type of SCI), pain treatment, and functional independence (Barthel Index) will be registered at the baseline measurement (t1). The participants complete a questionnaire on satisfaction with the program immediately after completion of the program at 3 months. Psychological variables: - Pain coping: Coping with Pain Questionnaire and Pain Coping Inventory List, and - Pain cognitions: Pain Cognition List.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)