A Cognitive-Behaviour Therapy (CBT) Self-Management Approach for Insomnia in Chronic Pain: A Randomized Control Trial

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2012 by Ottawa Hospital Research Institute.
Recruitment status was  Active, not recruiting
Sponsor:
Collaborator:
The Ottawa Hospital
Information provided by (Responsible Party):
Ottawa Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT01188460
First received: August 19, 2010
Last updated: March 1, 2012
Last verified: March 2012

August 19, 2010
March 1, 2012
April 2010
January 2012   (final data collection date for primary outcome measure)
  • Sleep Diary [ Time Frame: Timepoint 2 (week 7 of study participation). ] [ Designated as safety issue: No ]
    Measures Time in Bed, Total Sleep Time, Sleep Efficiency, Time to Fall Asleep, Total Number of Awakenings, and Sleep Quality
  • Insomnia Severity Index (ISI) [ Time Frame: Timepoint 2 (week 7 of study participation) ] [ Designated as safety issue: No ]
    Measures insomnia symptoms
Same as current
Complete list of historical versions of study NCT01188460 on ClinicalTrials.gov Archive Site
  • Pain Severity rating [ Time Frame: Timepoint 2 (week 7 of study participation). ] [ Designated as safety issue: No ]
    Measures pain severity
  • Pain Disability Index (PDI) [ Time Frame: Timepoint 2 (week 7 of study participation). ] [ Designated as safety issue: No ]
    Measures pain disability impact on various life domains
  • Hospital Anxiety and Depression Scale (HADS) [ Time Frame: Timepoint 2 (week 7 of study participation). ] [ Designated as safety issue: Yes ]
    Measures symptoms of depression and anxiety
  • Pre-Sleep Arousal Scale (PSAS) [ Time Frame: Timepoint 2 (week 7 of study participation). ] [ Designated as safety issue: No ]
    Measures pre-sleep hyperarousal
  • Fatigue Severity Scale (FSS) [ Time Frame: Timepoint 2 (week 7 of study participation). ] [ Designated as safety issue: No ]
    Measures symptoms of fatigue
Same as current
Not Provided
Not Provided
 
A Cognitive-Behaviour Therapy (CBT) Self-Management Approach for Insomnia in Chronic Pain: A Randomized Control Trial
A Cognitive-Behaviour Therapy (CBT) Self-Management Approach for Insomnia in Chronic Pain: A Randomized Control Trial

This study will test the impact of a cognitive-behavioural self-management approach for the management of insomnia among patients with chronic pain. This self-management approach consists of a manual describing cognitive behavioural techniques for the management of insomnia. In terms of primary outcomes, it is anticipated that there would be improvements in sleep-related dimensions such as sleep quality, sleep efficiency, and night-time awakenings in the sample group receiving a copy of the self-help manual intervention to be implemented by participants in their home (intervention group), relative to the group receiving treatment as usual (control group). In terms of secondary outcomes, it is anticipated that the intervention group will show improvements in mood, fatigue, pain severity, and pain-related disability relative to the control group. The tertiary outcome variable of pre-sleep arousal is anticipated to have a moderating or mediating relationship with the sleep variables investigated.

In summary therefore, insomnia and other sleep difficulties have been reported to frequently occur in conjunction with other medical or psychiatric disorders, however insomnia co-occurring with other medical or psychiatric conditions has received less attention relative to primary insomnia with no such concurrent conditions (e.g., Lichstein, 2006; McCrae, & Lichstein, 2001; Taylor, Mallory, Lichstein, Durrence, Riedel, & Bush, 2007). In chronic pain, there have not been many well-controlled studies involving insomnia existing with a concurrent chronically painful condition. Research thus far has found multi-component cognitive-behavioural approaches to be successful in treating primary insomnia, and there have been some studies applying these approaches in the context of insomnia and concurrent medical conditions (Currie, Wilson, Pontefract, & deLaplante, 2000; Morin, 1993). Based on Morin's work (Morin, 1993; Morin, Beaulieu-Bonneau, LeBlanc, & Savard, 2005) involving a cognitive-behaviour therapy (CBT) protocol for patients with sleep problems related to chronic pain, a self-help format of such an intervention has also been developed (Currie & Wilson, 1997). However, this has thus far only been delivered within a group-based treatment programme (Currie, 1998; Currie & Wilson, 1997; Currie, Wilson, Pontefract, & deLaplante, 2000). From this context, and building on a prior study involving a group treatment format (Currie, 1998; Currie, Wilson, Pontefract, & deLaplante, 2000), the usefulness of a manualized self-management approach in manageing insomnia will be investigated, including the impact of this approach with regard to other salient measures of improved functioning (such as pain severity or pain-related disability) for individuals with chronic pain. The proposed study will involve a randomized control trial of this self-help treatment strategy for comorbid insomnia in chronically painful medical conditions among an adult outpatient sample at a hospital rehabilitation centre and pain clinic. This study thus seeks to investigate how successful a cognitive-behaviour therapy (CBT) self-help management approach is for manageing insomnia amongst people with chronic pain. Given the public health implications of the relationship of poor sleep to quality of life (e.g., Morin, Stone, McDonald, & Jones, 1994; Quesnel, Savard, Simard, Ivers, & Morin, 2003), a self-management approach to insomnia in the context of chronic pain may offer an accessible and cost-effective treatment option.

The following hypotheses will be tested:

The first hypothesis predicts that participants in the intervention group will show changes in their scores on psychological measures in terms of greater improvements in sleep-related dimensions, in comparison with controls between the baseline and post-treatment periods.

The second hypothesis predicts that participants in the intervention group will show changes in their scores on psychological measures in terms of lower levels of anxiety, depression, fatigue, pain severity, and pain-related disability, in comparison with controls between the baseline and post-treatment periods. These secondary outcome variables are not directly targeted by the intervention, however it is proposed that if improvements in sleep are experienced, there would be subsequent improvements in the variables of mood, fatigue, pain severity, and pain-related disability among chronic pain patients who experience insomnia.

The third hypothesis predicts that the variable of pre-sleep arousal will have a moderating or mediating influence on the sleep-related variables (which will be the primary outcome variables). The moderating or mediating variable of pre-sleep arousal is proposed to assess dimensions related to sleep that are not tapped into by the primary outcome, sleep-related variables, but that may be of salience in the context of insomnia that is comorbid with chronically painful conditions.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Treatment
  • Insomnia
  • Chronic Pain
  • Behavioral: Sleep diary
    Completion of sleep diary in terms of time in bed, hours of sleep, time to fall asleep, number of awakenings, and sleep quality
    Other Names:
    • Wait-list control group
    • Treatment as usual group
  • Behavioral: Self-help manual for insomnia
    Implementation of chapters of self-help manual at home, and completion of sleep diary in terms of time in bed, hours of sleep, time to fall asleep, number of awakenings, and sleep quality
    Other Name: Intervention Group
  • Placebo Comparator: Control Group
    Receive one weekly telephone follow-up call per week to monitor sleep progress, complete 7 weeks of sleep diaries only, complete questionnaires at three study timepoints
    Intervention: Behavioral: Sleep diary
  • Experimental: Experimental Group
    Receive one weekly telephone call to monitor sleep progress, complete 7 weeks of sleep diaries, implement one chapter per week of self-help manual for insomnia over 7 weeks at home, complete questionnaires at three study timepoints
    Intervention: Behavioral: Self-help manual for insomnia
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
50
March 2012
January 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • 18 to 65 years of age
  • Not in state of crisis
  • Able to read and understand English
  • Experiences sleep difficulties or insomnia
  • Has chronic pain

Exclusion Criteria:

  • Under 18 or over 65 years of age
  • In a state of crisis
  • Does not read or understand English
  • Does not experience sleep difficulties or insomnia
  • Does not have chronic pain
Both
18 Years to 65 Years
Yes
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT01188460
2009902
No
Ottawa Hospital Research Institute
Ottawa Hospital Research Institute
The Ottawa Hospital
Principal Investigator: Keith E Wilson, PhD The Ottawa Hospital Rehabilitation Centre
Ottawa Hospital Research Institute
March 2012

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