Effect of Guided Imagery on Patients With Chronic Pain Related to Spinal Cord Injury

This study has been withdrawn prior to enrollment.
(Due to other projects priority)
Sponsor:
Information provided by (Responsible Party):
Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:
NCT00678548
First received: May 13, 2008
Last updated: April 7, 2015
Last verified: April 2015

May 13, 2008
April 7, 2015
October 2008
March 2009   (final data collection date for primary outcome measure)
Pain intensity [ Time Frame: four weeks ] [ Designated as safety issue: No ]
as measured by a numerical rating scale (daily) and Brief pain questionnaire (BPI) (baseline and after 4 weeks)
Pain intensity, as measured by NRS and BPIQ [ Time Frame: NRS daily and BPIQ pre and post, (four weeks ) ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00678548 on ClinicalTrials.gov Archive Site
BDI, BAI and SF36 [ Time Frame: pre and postintervention ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Effect of Guided Imagery on Patients With Chronic Pain Related to Spinal Cord Injury
Effect of Positive Guided Imagery on Patients With in or Below-level Chronic Pain Related to Spinal Cord Injury

Chronic pain after spinal cord injury in or below the level of injury is a common problem and can be severe.

The purpose of our study is to investigate the effect of pleasant guided imagery on spinal cord injured patients with chronic pain in or below the level of injury.

The study is a controlled simple blind randomized prospective study. Subjects who live in Trøndelag ( Norway) and who have a traumatic or non traumatic spinal cord injury with chronic pain in or below the level of injury will be included in the study.

Assessments: Pain will be measured with NRS(numeric pain rating scale) and BPIQ (Brief pain intervention questionnaire), anxiety and depression with BDI and BAI (Beck`s depression and anxiety inventory) and quality of live with SF36 health survey.

The subjects will be randomized in a treatment and control group. One group will use daily for four weeks a CD with a pleasant guided imagery, the other group will write a short pain diary.

The NRS will be registered daily and the other assessments before and after the interventions.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Treatment
Pain
  • Behavioral: Pleasant guided imagery
    CD with pleasant guided imagery
  • Behavioral: Pain diary
    Filling out a pain diary
  • Experimental: guided imagery
    CD
    Intervention: Behavioral: Pleasant guided imagery
  • Active Comparator: pain diary
    Pain diary
    Intervention: Behavioral: Pain diary
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
0
March 2009
March 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Traumatic and non traumatic SCI (spinal cord injury) persons in Trøndelag (Norway)

Exclusion Criteria:

  • Not sufficient knowledge of the Norwegian language, cancer, serious cognitive impairment, abuse or dependence of alcohol, narcotics or analgesics and dissociative disorder
Both
Child, Adult, Senior
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
Norway
 
NCT00678548
4.2007.1943
No
Not Provided
Not Provided
Norwegian University of Science and Technology
Norwegian University of Science and Technology
Not Provided
Principal Investigator: Gunnar Leivseth, Professor MD Norwegian University of Science and Technology
Norwegian University of Science and Technology
April 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP