Evaluation of a multidisciplinary cognitive behavioural programme for coping with chronic neuropathic pain following spinal cord injury.

Evaluation of a multidisciplinary cognitive behavioural programme for coping with chronic neuropathic pain following spinal cord injury: effects on pain intensity and pain related disability.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON27517

Enrollment

Registered

2008-12-11

Start date

2009-01-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

multidisciplinary behavioural program coping chronic neuropathic pain spinal cord injury multidisciplinair gedragsinterventie chronische neuropathische pijn dwarslaesie

Interventions

The multidisciplinary programme, comprising educational, cognitive, and behavioural interventions for coping with chronic neuropathic pain following spinal cord injury, consists of ten sessions of 3 h

2. guided group discussions

3. exercises and sport workshops

4. homework.

Eligibility

Inclusion criteria

Inclusion criteria: 1. Spinal cord injury; 2. at least 18 years old; 3. at least one year and at most ten years after discharge from first inpatient spinal cord injury rehabilitation; 4. informed consent; 5. main type of pain is neuropathic pain; 6. duration of neuropathic pain is at least six months; 7. pain intensity score at least 40 on the Chronic Pain Grade last week;

Exclusion criteria

Exclusion criteria: 1. Spinal cord injury by metastatic tumour; 2. former cognitive behavioural therapy for coping; 3. inability to function in a group by major language problems or psychopathology; 4. insufficient mastery of the Dutch. language

Design outcomes

Primary

Measure	Time frame
Pain intensity and pain related disability: Chronic Pain Grade questionnaire (CPG) at t1, t2, t3, t4, and t5.	—

Secondary

Measure	Time frame
Secondary outcome(s): 1. Level of activation and participation: Utrecht Activities List (UAL); 2. Life satisfaction: Life Satisfaction Questionnaire (LiSat-9); 3. Mood: Hospital Anxiety and Depression Scale (HADS); at t1, t2, t3, t4, and t5. Psychological variables: - Pain coping: Coping with Pain Questionnaire (CPV) and Pain Coping Inventory List (PCI) - Pain cognitions: Pain Cognition List (PCL-2003) at t1, t2, t3 (only intervention group) and t5 (only waiting list control group).	—

Measure

Time frame

Secondary outcome(s): 1. Level of activation and participation: Utrecht Activities List (UAL); 2. Life satisfaction: Life Satisfaction Questionnaire (LiSat-9); 3. Mood: Hospital Anxiety and Depression Scale (HADS); at t1, t2, t3, t4, and t5. Psychological variables: - Pain coping: Coping with Pain Questionnaire (CPV) and Pain Coping Inventory List (PCI) - Pain cognitions: Pain Cognition List (PCL-2003) at t1, t2, t3 (only intervention group) and t5 (only waiting list control group).

—

Contacts

Public ContactM. Heutink

Rembrandtkade 10

M.Heutink@dehoogstraat.nl+31 (0)30-2561211

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)