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OsteoArthritis and Therapy for Sleep (OATS)

Primary Purpose

Insomnia Related to Osteoarthritis Pain

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cognitive Behavior Therapy for Insomnia
Education Only Control
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Insomnia Related to Osteoarthritis Pain

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 60+ with one or more health care visits for OA in the prior 3 years
  • Score of ≥6 on 4-item ISI at first screening and ≥11 on full ISI at second screening
  • Score of ≥9 on two items from the Brief Pain Inventory (BPI) asking about average pain intensity in the past 2 weeks (0-10 scale) and activity interference due to pain (0-10 scale) at first and second screening

Exclusion Criteria:

  • Not continuously enrolled at Group Health Cooperative for at least one year
  • Prior diagnosis of a primary sleep disorder: sleep apnea with an AHI/RDI score of 15+ or current use of a CPAP machine; periodic leg movement disorder; restless leg syndrome; sleep-wake cycle disturbance; or rapid eye movement behavior disorder
  • Diagnosis in the medical record of: rheumatoid arthritis, terminal disease, being considered for major surgery, active chemotherapy or radiation for cancer, or inpatient treatment for congestive heart failure within the previous 6 months
  • Diagnosis of dementia, use of acetylcholinesterase inhibitor and/or memantine for cognitive impairment, or cognitive impairment (>6 on the Short Orientation-Memory-Concentration Test)
  • Hearing or speech impairment sufficient to preclude participation in a telephone intervention

Sites / Locations

  • Kaiser Permanente Washington Research Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Cognitive Behavioral Therapy

Education Control

Arm Description

Cognitive Behavioral Therapy for Insomnia is delivered by trained sleep therapists in six telephone sessions.

Education Only Control is delivered by trained sleep therapists in six telephone sessions.

Outcomes

Primary Outcome Measures

Insomnia Severity Index (ISI)
A 7-item questionnaire that is a global measure of perceived insomnia severity. Items use a 5-point scale for total scores of 0-28, with >15 considered moderate severity.

Secondary Outcome Measures

Insomnia Severity Index (ISI)
A 7-item questionnaire that is a global measure of perceived insomnia severity.Items use a 5-point scale for total scores of 0-28, with >15 considered moderate severity.
Pittsburgh Sleep Quality Index (PSQI)
Self-rating of overall sleep quality and disturbances using 7 sleep. components. PSQI global >5 is highly sensitive and specific for distinguishing good and poor sleepers.
Pittsburgh Sleep Quality Index (PSQI)
Self-rating of overall sleep quality and disturbances using 7 sleep components. PSQI global >5 is highly sensitive and specific for distinguishing good and poor sleepers.
Brief Pain Inventory-short form (BPI-sf)
A questionnaire to assess pain intensity and interference with activities. The BPI-sf rates pain intensity (4 items) and interference (7 items) from 0 to 10 and is validated for use in clinical trials with OA pain patients.
Brief Pain Inventory-short form (BPI-sf)
A questionnaire to assess pain intensity and interference with activities. The BPI-sf rates pain intensity (4 items) and interference (7 items) from 0 to 10 and is validated for use in clinical trials with OA pain patients.
Flinders Fatigue Scale (FFS)
A 7-item self-report questionnaire to measure fatigue level in a variety of situations.
Flinders Fatigue Scale (FFS)
A 7-item self-report questionnaire to measure fatigue level in a variety of situations.
Patient Health Questionnaire (PHQ-8)
4-point scale rates frequency of occurrence of 8 depressive symptoms.
Patient Health Questionnaire (PHQ-8)
4-point scale rates frequency of occurrence of 8 depressive symptoms.
Sleep Hygiene Index (SHI)
A 13-item scale that rates how often participants engage in specific sleep hygiene related behaviors, including continued adherence to CBT-I recommendations over time.
Sleep Hygiene Index (SHI)
A 13-item scale that rates how often participants engage in specific sleep hygiene related behaviors, including continued adherence to CBT-I recommendations over time.
EuroQoL 5D (EQ-5D)
Rates health status on five dimensions and overall health status from 0 to 100. The most widely used measure in clinical trials assessing general quality of life of OA patients.
EuroQoL 5D (EQ-5D)
Rates health status on five dimensions and overall health status from 0 to 100. The most widely used measure in clinical trials assessing general quality of life of OA patients.
Western Ontario and McMaster Universities Arthritis Index (WOMAC)
A 24-item questionnaire rating pain, stiffness, and physical functioning in everyday activities. It is the most widely used condition-specific quality of life measure for arthritis cost-effectiveness studies.
Western Ontario and McMaster Universities Arthritis Index (WOMAC)
A 24-item questionnaire rating pain, stiffness, and physical functioning in everyday activities. It is the most widely used condition-specific quality of life measure for arthritis cost-effectiveness studies.
Use of sleep and pain medications
NSAID, analgesic, sedative, and anti-depressant medication use.
Outpatient visits
The number of visits for OA, for sleep problems, and for visits irrespective of associated diagnosis.
Health care costs
The Group Health cost database will be used to estimate costs (from study entry to 24 months post enrollment) of ambulatory healthcare for all conditions, arthritis and sleep problems, and inpatient care.

Full Information

First Posted
October 19, 2016
Last Updated
April 1, 2020
Sponsor
University of Washington
Collaborators
Kaiser Permanente
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1. Study Identification

Unique Protocol Identification Number
NCT02946957
Brief Title
OsteoArthritis and Therapy for Sleep
Acronym
OATS
Official Title
Efficacy of Scalable CBT for Insomnia in Older Adults With Osteoarthritis Pain
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 2016 (undefined)
Primary Completion Date
December 2019 (Actual)
Study Completion Date
November 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
Kaiser Permanente

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Osteoarthritis (OA) pain affects 50 percent of older adults, more than half of whom also experience significant sleep disturbance. This randomized trial will determine whether a telephone-based cognitive behavioral treatment targeting insomnia in older adults with chronic severe OA-related insomnia and pain results in substantially greater reductions in insomnia severity and in related improvements in pain, fatigue, mood, quality of life and healthcare costs compared to telephone-delivered education (attention control) about insomnia. The trial will test an intervention that if demonstrated to have long term efficacy is scalable and has the potential for wide-scale deployment in healthcare systems.
Detailed Description
Twenty-five percent of older adults experience significant osteoarthritis (OA)-related comorbid sleep disturbance. Insomnia is associated with substantial negative effects on function, mood, and medical resource utilization. Cognitive behavioral therapy for insomnia (CBT-I) is evidence based and has been shown to be efficacious in populations with a variety of comorbid conditions including OA-related chronic pain. However, in-person CBT interventions are unlikely to be widely deployable in healthcare systems. Telephone delivery has the advantage of giving patients access to personalized, efficacious CBT-I interventions from home, increasing generalizability, and outreach to minority, rural, and other underserved populations. Older (60+ yrs) primary care patients across Washington State will be screened for severe persistent OA-related insomnia and pain. Two hundred and seventy patients will be randomized to either CBT-I or an education only attention control (EOC). Each treatment will consist of six 20-30 minute telephone-based sessions over an eight week period. Pre-treatment, post-treatment (2 months and 12 month) assessments will include measures of sleep, pain, fatigue, mood, and quality of life. A cost effectiveness evaluation of the intervention will also be conducted. The proposed research will determine if telephone CBT-I improves OA insomnia and associated outcomes in a state-wide primary care population of older adults, and inform policy decisions about widespread dissemination of telephone CBT-I in this and related patient populations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insomnia Related to Osteoarthritis Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
327 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cognitive Behavioral Therapy
Arm Type
Experimental
Arm Description
Cognitive Behavioral Therapy for Insomnia is delivered by trained sleep therapists in six telephone sessions.
Arm Title
Education Control
Arm Type
Active Comparator
Arm Description
Education Only Control is delivered by trained sleep therapists in six telephone sessions.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Behavior Therapy for Insomnia
Other Intervention Name(s)
CBT-I
Intervention Description
Six telephone sessions that last 20-30 minutes presenting cognitive behavioral therapy for insomnia.
Intervention Type
Behavioral
Intervention Name(s)
Education Only Control
Other Intervention Name(s)
EOC
Intervention Description
Six telephone sessions that last 20-30 minutes presenting sleep and osteoarthritis education.
Primary Outcome Measure Information:
Title
Insomnia Severity Index (ISI)
Description
A 7-item questionnaire that is a global measure of perceived insomnia severity. Items use a 5-point scale for total scores of 0-28, with >15 considered moderate severity.
Time Frame
12 months post baseline
Secondary Outcome Measure Information:
Title
Insomnia Severity Index (ISI)
Description
A 7-item questionnaire that is a global measure of perceived insomnia severity.Items use a 5-point scale for total scores of 0-28, with >15 considered moderate severity.
Time Frame
2 months post baseline
Title
Pittsburgh Sleep Quality Index (PSQI)
Description
Self-rating of overall sleep quality and disturbances using 7 sleep. components. PSQI global >5 is highly sensitive and specific for distinguishing good and poor sleepers.
Time Frame
2 months post baseline
Title
Pittsburgh Sleep Quality Index (PSQI)
Description
Self-rating of overall sleep quality and disturbances using 7 sleep components. PSQI global >5 is highly sensitive and specific for distinguishing good and poor sleepers.
Time Frame
12 months post baseline
Title
Brief Pain Inventory-short form (BPI-sf)
Description
A questionnaire to assess pain intensity and interference with activities. The BPI-sf rates pain intensity (4 items) and interference (7 items) from 0 to 10 and is validated for use in clinical trials with OA pain patients.
Time Frame
2 months post baseline
Title
Brief Pain Inventory-short form (BPI-sf)
Description
A questionnaire to assess pain intensity and interference with activities. The BPI-sf rates pain intensity (4 items) and interference (7 items) from 0 to 10 and is validated for use in clinical trials with OA pain patients.
Time Frame
12 months post baseline
Title
Flinders Fatigue Scale (FFS)
Description
A 7-item self-report questionnaire to measure fatigue level in a variety of situations.
Time Frame
2 months post baseline
Title
Flinders Fatigue Scale (FFS)
Description
A 7-item self-report questionnaire to measure fatigue level in a variety of situations.
Time Frame
12 months post baseline
Title
Patient Health Questionnaire (PHQ-8)
Description
4-point scale rates frequency of occurrence of 8 depressive symptoms.
Time Frame
2 months post baseline
Title
Patient Health Questionnaire (PHQ-8)
Description
4-point scale rates frequency of occurrence of 8 depressive symptoms.
Time Frame
12 months post baseline
Title
Sleep Hygiene Index (SHI)
Description
A 13-item scale that rates how often participants engage in specific sleep hygiene related behaviors, including continued adherence to CBT-I recommendations over time.
Time Frame
2 months post baseline
Title
Sleep Hygiene Index (SHI)
Description
A 13-item scale that rates how often participants engage in specific sleep hygiene related behaviors, including continued adherence to CBT-I recommendations over time.
Time Frame
12 months post baseline
Title
EuroQoL 5D (EQ-5D)
Description
Rates health status on five dimensions and overall health status from 0 to 100. The most widely used measure in clinical trials assessing general quality of life of OA patients.
Time Frame
2 months post baseline
Title
EuroQoL 5D (EQ-5D)
Description
Rates health status on five dimensions and overall health status from 0 to 100. The most widely used measure in clinical trials assessing general quality of life of OA patients.
Time Frame
12 months post baseline
Title
Western Ontario and McMaster Universities Arthritis Index (WOMAC)
Description
A 24-item questionnaire rating pain, stiffness, and physical functioning in everyday activities. It is the most widely used condition-specific quality of life measure for arthritis cost-effectiveness studies.
Time Frame
2 months post baseline
Title
Western Ontario and McMaster Universities Arthritis Index (WOMAC)
Description
A 24-item questionnaire rating pain, stiffness, and physical functioning in everyday activities. It is the most widely used condition-specific quality of life measure for arthritis cost-effectiveness studies.
Time Frame
12 months post baseline
Title
Use of sleep and pain medications
Description
NSAID, analgesic, sedative, and anti-depressant medication use.
Time Frame
Baseline through 24 months
Title
Outpatient visits
Description
The number of visits for OA, for sleep problems, and for visits irrespective of associated diagnosis.
Time Frame
Baseline through 24 months
Title
Health care costs
Description
The Group Health cost database will be used to estimate costs (from study entry to 24 months post enrollment) of ambulatory healthcare for all conditions, arthritis and sleep problems, and inpatient care.
Time Frame
Baseline through 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 60+ with one or more health care visits for OA in the prior 3 years Score of ≥6 on 4-item ISI at first screening and ≥11 on full ISI at second screening Score of ≥9 on two items from the Brief Pain Inventory (BPI) asking about average pain intensity in the past 2 weeks (0-10 scale) and activity interference due to pain (0-10 scale) at first and second screening Exclusion Criteria: Not continuously enrolled at Group Health Cooperative for at least one year Prior diagnosis of a primary sleep disorder: sleep apnea with an AHI/RDI score of 15+ or current use of a CPAP machine; periodic leg movement disorder; restless leg syndrome; sleep-wake cycle disturbance; or rapid eye movement behavior disorder Diagnosis in the medical record of: rheumatoid arthritis, terminal disease, being considered for major surgery, active chemotherapy or radiation for cancer, or inpatient treatment for congestive heart failure within the previous 6 months Diagnosis of dementia, use of acetylcholinesterase inhibitor and/or memantine for cognitive impairment, or cognitive impairment (>6 on the Short Orientation-Memory-Concentration Test) Hearing or speech impairment sufficient to preclude participation in a telephone intervention
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael V Vitiello, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Susan M McCurry, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michael Von Korff, ScD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kai Yeung, PhD
Organizational Affiliation
Kaiser Permanente
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kaiser Permanente Washington Research Institute
City
Seattle
State/Province
Washington
ZIP/Postal Code
98101
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34516646
Citation
Vitiello MV, Zhu W, Von Korff M, Wellman R, Morin CM, Yeung K, McCurry SM. Long-term improvements in sleep, pain, depression, and fatigue in older adults with comorbid osteoarthritis pain and insomnia. Sleep. 2022 Feb 14;45(2):zsab231. doi: 10.1093/sleep/zsab231.
Results Reference
derived
PubMed Identifier
33910159
Citation
Thakral M, Von Korff M, McCurry SM, Morin CM, Vitiello MV. ISI-3: evaluation of a brief screening tool for insomnia. Sleep Med. 2021 Jun;82:104-109. doi: 10.1016/j.sleep.2020.08.027. Epub 2020 Aug 27.
Results Reference
derived
PubMed Identifier
33616613
Citation
McCurry SM, Zhu W, Von Korff M, Wellman R, Morin CM, Thakral M, Yeung K, Vitiello MV. Effect of Telephone Cognitive Behavioral Therapy for Insomnia in Older Adults With Osteoarthritis Pain: A Randomized Clinical Trial. JAMA Intern Med. 2021 Apr 1;181(4):530-538. doi: 10.1001/jamainternmed.2020.9049.
Results Reference
derived
PubMed Identifier
31614214
Citation
McCurry SM, Von Korff M, Morin CM, Cunningham A, Pike KC, Thakral M, Wellman R, Yeung K, Zhu W, Vitiello MV. Telephone interventions for co-morbid insomnia and osteoarthritis pain: The OsteoArthritis and Therapy for Sleep (OATS) randomized trial design. Contemp Clin Trials. 2019 Dec;87:105851. doi: 10.1016/j.cct.2019.105851. Epub 2019 Oct 13.
Results Reference
derived

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OsteoArthritis and Therapy for Sleep

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