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

Primary Purpose

Insomnia, Chronic Pain

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Self-help manual for insomnia
Sleep diary
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia focused on measuring Insomnia, Chronic pain

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • The Ottawa Hospital, Pain Clinic
  • The Ottawa Hospital Rehabilitation Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Control Group

Experimental Group

Arm Description

Receive one weekly telephone follow-up call per week to monitor sleep progress, complete 7 weeks of sleep diaries only (sleep diary measures Total Sleep Time in hours, Time to Fall Asleep in minutes, Number of Nocturnal Awakenings, Sleep Efficiency as a percentage, and Sleep Quality as units on a scale), complete questionnaires at three study timepoints

Receive one weekly telephone call to monitor sleep progress, complete 7 weeks of sleep diaries (sleep diary measures Total Sleep Time in hours, Time to Fall Asleep in minutes, Number of Nocturnal Awakenings, Sleep Efficiency as a percentage, and Sleep Quality as units on a scale), implement one chapter per week of self-help manual for insomnia over 7 weeks at home, complete questionnaires at three study timepoints

Outcomes

Primary Outcome Measures

Insomnia Severity Index (ISI)
Measures insomnia symptoms, scores range from 0-28 with higher scores (ranging from 15-28) indicating clinical insomnia and therefore worse outcomes
Sleep Diary- Total Sleep Time
Measures: Total Sleep Time in hours, higher scores indicate better outcomes
Sleep Diary- Time to Fall Asleep
Measures: Time to Fall Asleep in minutes, higher scores indicate worse outcomes
Sleep Diary- Number of Nocturnal Awakenings
Measures: Number of Nocturnal Awakenings, higher scores indicate worse outcomes
Sleep Diary- Sleep Efficiency
Measures: Sleep Efficiency (percentage)- higher scores indicate better outcomes
Sleep Diary- Sleep Quality
Measures: Sleep Quality (units on a scale from 0-10), higher scores indicate better outcomes

Secondary Outcome Measures

Pain Severity Rating
Measures pain severity, rated on scale from 0-10, total scores range from 0-40, higher scores indicate worse outcomes
Pain Disability Index (PDI)
Measures pain disability impact on various life domains, scores range from 0-70, higher scores indicate worse outcomes
Hospital Anxiety and Depression Scale (HADS)
Measures symptoms of depression and anxiety, total scores range from 0-42, higher scores indicate worse outcomes
Pre-Sleep Arousal Scale (PSAS)
Measures pre-sleep hyperarousal, total scores range from 16-80, higher scores indicate worse outcomes
Fatigue Severity Scale (FSS)
Measures symptoms of fatigue, total scores range from 9-63, higher scores indicate worse outcomes

Full Information

First Posted
August 19, 2010
Last Updated
August 10, 2017
Sponsor
Ottawa Hospital Research Institute
Collaborators
The Ottawa Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01188460
Brief Title
A Cognitive-Behaviour Therapy (CBT) Self-Management Approach for Insomnia in Chronic Pain: A Randomized Control Trial
Official Title
A Cognitive-Behaviour Therapy (CBT) Self-Management Approach for Insomnia in Chronic Pain: A Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
April 2010 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
March 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ottawa Hospital Research Institute
Collaborators
The Ottawa Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia, Chronic Pain
Keywords
Insomnia, Chronic pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
Placebo Comparator
Arm Description
Receive one weekly telephone follow-up call per week to monitor sleep progress, complete 7 weeks of sleep diaries only (sleep diary measures Total Sleep Time in hours, Time to Fall Asleep in minutes, Number of Nocturnal Awakenings, Sleep Efficiency as a percentage, and Sleep Quality as units on a scale), complete questionnaires at three study timepoints
Arm Title
Experimental Group
Arm Type
Experimental
Arm Description
Receive one weekly telephone call to monitor sleep progress, complete 7 weeks of sleep diaries (sleep diary measures Total Sleep Time in hours, Time to Fall Asleep in minutes, Number of Nocturnal Awakenings, Sleep Efficiency as a percentage, and Sleep Quality as units on a scale), implement one chapter per week of self-help manual for insomnia over 7 weeks at home, complete questionnaires at three study timepoints
Intervention Type
Behavioral
Intervention Name(s)
Self-help manual for insomnia
Other Intervention Name(s)
Intervention Group
Intervention Description
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
Intervention Type
Behavioral
Intervention Name(s)
Sleep diary
Primary Outcome Measure Information:
Title
Insomnia Severity Index (ISI)
Description
Measures insomnia symptoms, scores range from 0-28 with higher scores (ranging from 15-28) indicating clinical insomnia and therefore worse outcomes
Time Frame
Timepoint 2 (week 7 of study participation)
Title
Sleep Diary- Total Sleep Time
Description
Measures: Total Sleep Time in hours, higher scores indicate better outcomes
Time Frame
Timepoint 2 (week 7 of study participation).
Title
Sleep Diary- Time to Fall Asleep
Description
Measures: Time to Fall Asleep in minutes, higher scores indicate worse outcomes
Time Frame
Timepoint 2 (week 7 of study participation).
Title
Sleep Diary- Number of Nocturnal Awakenings
Description
Measures: Number of Nocturnal Awakenings, higher scores indicate worse outcomes
Time Frame
Timepoint 2 (week 7 of study participation).
Title
Sleep Diary- Sleep Efficiency
Description
Measures: Sleep Efficiency (percentage)- higher scores indicate better outcomes
Time Frame
Timepoint 2 (week 7 of study participation).
Title
Sleep Diary- Sleep Quality
Description
Measures: Sleep Quality (units on a scale from 0-10), higher scores indicate better outcomes
Time Frame
Timepoint 2 (week 7 of study participation).
Secondary Outcome Measure Information:
Title
Pain Severity Rating
Description
Measures pain severity, rated on scale from 0-10, total scores range from 0-40, higher scores indicate worse outcomes
Time Frame
Timepoint 2 (week 7 of study participation).
Title
Pain Disability Index (PDI)
Description
Measures pain disability impact on various life domains, scores range from 0-70, higher scores indicate worse outcomes
Time Frame
Timepoint 2 (week 7 of study participation).
Title
Hospital Anxiety and Depression Scale (HADS)
Description
Measures symptoms of depression and anxiety, total scores range from 0-42, higher scores indicate worse outcomes
Time Frame
Timepoint 2 (week 7 of study participation).
Title
Pre-Sleep Arousal Scale (PSAS)
Description
Measures pre-sleep hyperarousal, total scores range from 16-80, higher scores indicate worse outcomes
Time Frame
Timepoint 2 (week 7 of study participation).
Title
Fatigue Severity Scale (FSS)
Description
Measures symptoms of fatigue, total scores range from 9-63, higher scores indicate worse outcomes
Time Frame
Timepoint 2 (week 7 of study participation).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Keith E Wilson, PhD
Organizational Affiliation
The Ottawa Hospital Rehabilitation Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Ottawa Hospital, Pain Clinic
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L6
Country
Canada
Facility Name
The Ottawa Hospital Rehabilitation Centre
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8M2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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

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