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Stepped Care Model for the Wider Dissemination of Cognitive-Behavioural Therapy for Insomnia Among Cancer Patients (Stepped Care)

Primary Purpose

Insomnia

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Professionally-administered cognitive-behavioral therapy for insomnia (CBT-I)
Web-based cognitive-behavioral therapy for insomnia (CBT-I)
Sponsored by
CHU de Quebec-Universite Laval
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia focused on measuring stepped care model, insomnia, cancer, cognitive-behavioural therapy, self-help treatment, web-based intervention, non-inferiority design, cost-effectiveness

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • have received a diagnosis of non-metastatic cancer (any type) in the past -18 months
  • to have an ISI score > 7
  • to be aged between 18 and 75 years old
  • to be readily able to read and understand French

Exclusion Criteria:

  • having a life expectancy < 1 year
  • having a severe psychiatric disorder (e.g., psychotic, substance use, severe depressive disorder)
  • having severe cognitive impairments (e.g., diagnosis of Parkinson's disease, dementia, or Mini-Mental State Examination score < 24)
  • having received a formal diagnosis for another sleep disorder (e.g., obstructive sleep apnea, periodic limb movement disorder)
  • shift work in the past 3 months or in the next 12 months
  • to have received a CBT for insomnia in the past

Sites / Locations

  • Centre de recherche de L'Hôtel-Dieu de Québec

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Professionally Administered CBT-I (Standard Care)

Stepped Care CBT-I

Arm Description

Patients (n = 59) assigned to this group will receive 6 weekly sessions of cognitive-behavioral therapy for insomnia (CBT-I) of approximately 50 minutes, offered individually by a licensed psychologist with significant experience (at least 2 years) in the administration of CBT-I with cancer patients.

Patients having an ISI score > 7 but < 15 (n = 65), will all receive first a web-based CBT-I for six weeks. Each week, the patients will first have to read written information on the website, and then watch a video capsule (duration between 5 and 20 min each). Patients with an ISI score > 14 (n = 53) will receive six weekly sessions of CBT-I administered individually by a professional.

Outcomes

Primary Outcome Measures

Change in Insomnia Severity Index
total score
Change in sleep efficiency (SE) index (%)
total sleep time/total time spent in bed X 100 - from sleep diary

Secondary Outcome Measures

Change in sleep onset latency (SOL) - from sleep diary
time to sleep after lights out - from sleep diary
Change in wake after sleep onset (WASO) - from sleep diary
summation of nocturnal awakenings - from sleep diary
Change in total wake time (TWT) - from sleep diary
summation of SOL, WASO, and early morning awakening - from sleep diary
Change in total sleep time (TST) - from sleep diary
time in bed minus total wake time - from sleep diary
Change in hypnotic use - from sleep diary
use of sleep-promoting medications - from sleep diary
Change in sleep onset latency (SOL) - from actigraphy
time to sleep after lights out - from actigraphy
Change in wake after sleep onset (WASO) - from actigraphy
summation of nocturnal awakenings - from actigraphy
Change in total wake time (TWT) - from actigraphy
summation of SOL, WASO, and early morning awakening - from actigraphy
Change in total sleep time (TST) - from actigraphy
time in bed minus total wake time - from actigraphy
Change in sleep efficiency (SE) index (%) - from actigraphy
ratio of total sleep time to the actual time spent in bed multiplied by 100

Full Information

First Posted
May 21, 2013
Last Updated
March 11, 2022
Sponsor
CHU de Quebec-Universite Laval
Collaborators
Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT01864720
Brief Title
Stepped Care Model for the Wider Dissemination of Cognitive-Behavioural Therapy for Insomnia Among Cancer Patients
Acronym
Stepped Care
Official Title
A Stepped Care Model for the Wider Dissemination of Cognitive-Behavioural Therapy for Insomnia Among Cancer Patients : Efficacy and Cost-Effectiveness.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
November 2018 (Actual)
Study Completion Date
November 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
CHU de Quebec-Universite Laval
Collaborators
Canadian Institutes of Health Research (CIHR)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Insomnia is very common in cancer patients. When left untreated, insomnia can lead to numerous serious consequences (e.g., psychological disorders) for the individual and significant costs for society (e.g., increased medical consultations). Cognitive-behavioural therapy (CBT), a form of psychotherapy, is now considered the treatment of choice for insomnia and its efficacy has been demonstrated in clinical studies conducted in cancer patients. Unfortunately, CBT for insomnia (CBT-I) is not widely accessible as only a few cancer clinics have mental health professionals formally trained in the administration of this treatment. Innovative models of treatment delivery are therefore needed to make sure that every cancer patient with insomnia receives the care he/she needs. A stepped care approach in which patients only receive the level of treatment that they need, beginning with a minimal, less costly, intervention followed by more intensive treatment if required, has shown some promises for other psychological disorders (e.g., depression). Although its relevance has been emphasized to make CBT-I more accessible, its utility has never been investigated. The main goal of this randomized non-inferiority study is to assess the efficacy and costeffectiveness of a stepped care CBT-I as compared with standard care. Our hypothesis is that a stepped care approach will not be statistically inferior in terms of efficacy as compared to usual care, while being much less costly (better cost-effectiveness ratio). Three hundred cancer patients (mixed cancer sites) with insomnia symptoms will be assigned to: (1) stepped care CBT-I (n = 118) or (2) standard care (n = 59), consisting of 6 weekly sessions administered individually by a professional.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia
Keywords
stepped care model, insomnia, cancer, cognitive-behavioural therapy, self-help treatment, web-based intervention, non-inferiority design, cost-effectiveness

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
177 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Professionally Administered CBT-I (Standard Care)
Arm Type
Active Comparator
Arm Description
Patients (n = 59) assigned to this group will receive 6 weekly sessions of cognitive-behavioral therapy for insomnia (CBT-I) of approximately 50 minutes, offered individually by a licensed psychologist with significant experience (at least 2 years) in the administration of CBT-I with cancer patients.
Arm Title
Stepped Care CBT-I
Arm Type
Experimental
Arm Description
Patients having an ISI score > 7 but < 15 (n = 65), will all receive first a web-based CBT-I for six weeks. Each week, the patients will first have to read written information on the website, and then watch a video capsule (duration between 5 and 20 min each). Patients with an ISI score > 14 (n = 53) will receive six weekly sessions of CBT-I administered individually by a professional.
Intervention Type
Behavioral
Intervention Name(s)
Professionally-administered cognitive-behavioral therapy for insomnia (CBT-I)
Intervention Description
The treatment content will be the same whether it is administered by a professional or self-administered. This multimodal approach combines behavioural (i.e., stimulus control therapy, sleep restriction), cognitive (i.e., cognitive restructuring), and educational (i.e., sleep hygiene) strategies that are administered over a 6-week period.
Intervention Type
Behavioral
Intervention Name(s)
Web-based cognitive-behavioral therapy for insomnia (CBT-I)
Other Intervention Name(s)
Self-administered
Intervention Description
The treatment content will be the same whether it is administered by a professional or self-administered. Each week, the patients will first have to read written information on the website, and then watch a video capsule (duration between 5 and 20 min each). The treatment material will be identical to the video (DVD)-based CBT-I that we previously developed. Patients will complete their daily sleep diary electronically on the website and the content will be interactive. It will include the sending of automated emails to remind participants to complete the treatment tasks and encourage adherence, provision of tailored feedback (e.g., texts, charts) based on the information that they provide in their sleep diary, as well as quizzes with automated correction to reinforce patients' understanding of the content.
Primary Outcome Measure Information:
Title
Change in Insomnia Severity Index
Description
total score
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Title
Change in sleep efficiency (SE) index (%)
Description
total sleep time/total time spent in bed X 100 - from sleep diary
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Secondary Outcome Measure Information:
Title
Change in sleep onset latency (SOL) - from sleep diary
Description
time to sleep after lights out - from sleep diary
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Title
Change in wake after sleep onset (WASO) - from sleep diary
Description
summation of nocturnal awakenings - from sleep diary
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Title
Change in total wake time (TWT) - from sleep diary
Description
summation of SOL, WASO, and early morning awakening - from sleep diary
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Title
Change in total sleep time (TST) - from sleep diary
Description
time in bed minus total wake time - from sleep diary
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Title
Change in hypnotic use - from sleep diary
Description
use of sleep-promoting medications - from sleep diary
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Title
Change in sleep onset latency (SOL) - from actigraphy
Description
time to sleep after lights out - from actigraphy
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Title
Change in wake after sleep onset (WASO) - from actigraphy
Description
summation of nocturnal awakenings - from actigraphy
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Title
Change in total wake time (TWT) - from actigraphy
Description
summation of SOL, WASO, and early morning awakening - from actigraphy
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Title
Change in total sleep time (TST) - from actigraphy
Description
time in bed minus total wake time - from actigraphy
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)
Title
Change in sleep efficiency (SE) index (%) - from actigraphy
Description
ratio of total sleep time to the actual time spent in bed multiplied by 100
Time Frame
Pre-tx (at recruitment; T1), post-tx (6 weeks after; T2), 3-month FU (T3), 6-month FU (T4), 12-month FU (T5)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: have received a diagnosis of non-metastatic cancer (any type) in the past -18 months to have an ISI score > 7 to be aged between 18 and 75 years old to be readily able to read and understand French Exclusion Criteria: having a life expectancy < 1 year having a severe psychiatric disorder (e.g., psychotic, substance use, severe depressive disorder) having severe cognitive impairments (e.g., diagnosis of Parkinson's disease, dementia, or Mini-Mental State Examination score < 24) having received a formal diagnosis for another sleep disorder (e.g., obstructive sleep apnea, periodic limb movement disorder) shift work in the past 3 months or in the next 12 months to have received a CBT for insomnia in the past
Facility Information:
Facility Name
Centre de recherche de L'Hôtel-Dieu de Québec
City
Québec
ZIP/Postal Code
G1R 2J6
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
20041590
Citation
Espie CA. "Stepped care": a health technology solution for delivering cognitive behavioral therapy as a first line insomnia treatment. Sleep. 2009 Dec;32(12):1549-58. doi: 10.1093/sleep/32.12.1549.
Results Reference
background
PubMed Identifier
18591549
Citation
Espie CA, Fleming L, Cassidy J, Samuel L, Taylor LM, White CA, Douglas NJ, Engleman HM, Kelly HL, Paul J. Randomized controlled clinical effectiveness trial of cognitive behavior therapy compared with treatment as usual for persistent insomnia in patients with cancer. J Clin Oncol. 2008 Oct 1;26(28):4651-8. doi: 10.1200/JCO.2007.13.9006. Epub 2008 Jun 30. Erratum In: J Clin Oncol. 2010 Jul 1;28(19):3205.
Results Reference
background
PubMed Identifier
16135475
Citation
Savard J, Simard S, Ivers H, Morin CM. Randomized study on the efficacy of cognitive-behavioral therapy for insomnia secondary to breast cancer, part I: Sleep and psychological effects. J Clin Oncol. 2005 Sep 1;23(25):6083-96. doi: 10.1200/JCO.2005.09.548.
Results Reference
background
PubMed Identifier
34228123
Citation
Savard J, Ivers H, Savard MH, Morin CM, Caplette-Gingras A, Bouchard S, Lacroix G. Efficacy of a stepped care approach to deliver cognitive-behavioral therapy for insomnia in cancer patients: a noninferiority randomized controlled trial. Sleep. 2021 Nov 12;44(11):zsab166. doi: 10.1093/sleep/zsab166.
Results Reference
derived

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Stepped Care Model for the Wider Dissemination of Cognitive-Behavioural Therapy for Insomnia Among Cancer Patients

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