The Efficacy of CBT-I in Alcoholics & Its Effects on Remission & Relapse

Sponsor
VA Office of Research and Development (U.S. Fed)
Overall Status
Completed
CT.gov ID
NCT01987089
Collaborator
University of Pennsylvania (Other), University of Michigan (Other)
63
1
2
67.5
0.9

Study Details

Study Description

Brief Summary

Insomnia is a highly prevalent disorder in those recovering from alcoholism. It has been associated with anxiety and depressive symptoms, as well as an increased risk of relapse back to the drinking.

Cognitive Behavioral Therapy for Insomnia (CBT-I), a non-pharmacologic approach is the recommended standard of care for insomnia. Some preliminary studies have shown that CBT-I may be efficacious for insomnia during recovery.

The current study proposes to use a standard 8-week CBT-I to treat the insomnia with a post-treatment follow-up at 3- and 6-months (after treatment). Further, it will evaluate if an improvement in the insomnia is associated with an improvement in the underling alcoholism and the daytime functioning. On an exploratory basis, the association of a first-degree family history of alcoholism with the insomnia severity and treatment response will also be evaluated.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive Behavioral Therapy for Insomnia (CBT-I)
N/A

Detailed Description

Eligible subjects will be Veterans with alcohol dependence during their first year of recovery, 21-65 years old, with ISI total score of 15 or more, medically and psychiatrically stable, and without dependence on other drugs (with the exception of nicotine and marijuana).

The proposed study will consist of a single-blind trial comparing CBT-I against a behavioral placebo intervention (Quasi-Desensitization Therapy, QDT).

Baseline assessments conducted over a month will comprehensively evaluate for the addiction, psychiatric, sleep and medical disorders, as well as for a family history of alcohol dependence.

Once the subject is seen to be eligible for the study he will be randomized to either the CBT-I or the QDT arm, and treated for the next weeks. The primary outcome measure for insomnia will be the Insomnia Severity Index. The primary outcome measure for alcohol dependence will be the percent days abstinent (on the Time Line Follow Back measure, TLFB), and the daytime symptoms will be assessed using the Short Form-12 item scale (SF-12, for self reported well-being), the Beck Depression Inventory (BDI, for depressive symptoms), and the State Trait Anxiety Inventory (STAI, for anxiety symptoms).

After completion of the treatment phase, subjects will be followed up 3 months and 6 months later, to assess for changes over time in their insomnia, alcohol use, and daytime functioning.

Study Design

Study Type:
Interventional
Actual Enrollment :
63 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
The Efficacy of CBT-I in Alcoholics & Its Effects on Remission & Relapse
Actual Study Start Date :
Aug 15, 2014
Actual Primary Completion Date :
May 23, 2019
Actual Study Completion Date :
Mar 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: CBT-I

Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. Session 1 serves as an orientation. No active treatment is delivered at this time. Sessions 2 & 3 are used to deliver the three main components of the intervention which are Sleep Restriction (SRT), Stimulus Control, and Sleep Hygiene. All but two of the remaining sessions are dedicated to the titration of total sleep time and to ensuring patient adherence. One session (session 5) entails the delivery of a specific form of cognitive therapy. The final session (session 8) is used to engage in a relapse-prevention didactic, i.e., to review first, how insomnia becomes chronic and second, the strategies that are likely to abort an extended episode of insomnia.

Behavioral: Cognitive Behavioral Therapy for Insomnia (CBT-I)
Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician.

Placebo Comparator: QDT

This form of placebo therapy has been commonly used in prior studies investigating behavioral interventions for insomnia. The therapist presents the QDT as a means to eliminate "conditioned arousal," occurring after nocturnal arousal using 8 sessions on a weekly basis. The therapist initially helps the subject to develop a chronological 12-item hierarchy of commonly practiced activities on awakening at night, like opening eyes and clock watching. As a next step, the subject develops 6 imaginable scenes of himself/herself engaged in neutral activities like reading a newspaper. The therapist then helps the subject pair the neutral scenes with the items from the 12-item hierarchy, which is then practiced by the subject 2 hours before bedtime.

Behavioral: Cognitive Behavioral Therapy for Insomnia (CBT-I)
Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician.

Outcome Measures

Primary Outcome Measures

  1. Change in Insomnia Severity Index - Total Score [8 weeks, 3 months post-treatment, and 6 months post-treatment]

    Insomnia Severity Index (ISI): This 7-item (0-4 Likert scales) measure yields a total score of 28. The norms for the scale are as follows: 0-7 represents no clinically significant insomnia; 8-14 represents sub threshold insomnia; 15-21 represents clinical insomnia (moderate severity); 21-28 represents clinical insomnia (severe). The scale provides a measure of severity of insomnia (overall), a measure of insomnia subtype, a measure of the diurnal effects of insomnia, and a measure of sleep "satisfaction". The ISI will be completed at baseline and for all the subsequent study-related visits.

  2. Change in Percent Days Abstinent (PDA) on the Time Line Follow Back Measure [8 weeks, 3 months post-treatment and 6-months post-treatment]

    Time Line Follow Back measure (TLFB): The TLFB provides assessment of drinking using a calendar format for the number of standard alcoholic beverages consumed per day. A standard drink, as defined by the National Institutes of Health, is 12 oz of regular beer, 5 oz of regular wine, or 1.5 oz of distilled spirits (e.g. whiskey). Numerous indices may be derived from the TLFB, such as the Percent Days Abstinent (PDA) proposed in this study. The PDA is derived as the percentage of days an individual reports being abstinent from alcohol within a given assessment time period.

Other Outcome Measures

  1. Change in PCS From the Short Form - 12 Item (SF-12) Measure [8 weeks, 3 months post-treatment, and 6 months post-treatment]

    The Physical Component Summary (PCS) scale has a range from 0 (indicating the lowest level of health) to 100 (indicating the best level of health).

  2. Change in MCS From the Short Form - 12 Item (SF-12) Measure [8 weeks, 3 months post-treatment, and 6 months post-treatment]

    The Mental Component Summary (MCS) scale has a range from 0 (indicating the lowest level of health) to 100 (indicating the best level of health).

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Male and female Veterans between the ages of 21 and 70 years

  • DSM IV diagnosis of alcohol dependence over the past year (as determined by the Structured Clinical Interview for DSM-IV Axis I Disorders [SCID-I])

  • Self-reported sleep latency or wake time after sleep onset >30 min on three or more nights per week for 1 month and a score of 15 or more on the Insomnia Severity Index (ISI)

  • No current alcohol withdrawal symptoms at baseline: CIWA score < 8 (CIWA is the Clinical Institute Withdrawal Assessment scale for alcohol withdrawal signs and symptoms)

  • Abstain for at least 4 weeks from heavy drinking, and < 12 months of abstinence from heavy drinking prior to the baseline study assessments, as assessed by subjective report or breathalyzer

  • Ability to speak, understand and print in English

  • Capacity to give written informed consent

Exclusion Criteria:
  • DSM-IV criteria for dependence on any other substance including benzodiazepines (and excluding nicotine dependence)

  • Positive urine drug screen for opioids, cocaine, or amphetamine (positive screen for Tetra Hydro Cannabinol is not considered an exclusion criteria)

  • Patient is currently in alcohol withdrawal as assessed by the Clinical Institute Withdrawal Assessment Scale (CIWA) total score of 8 or more

  • A lifetime DSM-IV diagnosis of Bipolar I or II disorder, Schizophrenia, or other psychotic disorder, as determined on the SCID-I, and current (past month) DSM-IV diagnosis of Major Depressive Disorder

  • Presence of unstable medical diagnosis e.g. congestive heart failure, leading to interference with sleep, as reported on history, examination, and/or review of clinical chart during baseline assessments

  • Current use of any medications that may influence the drinking behavior, e.g. naltrexone or acamprosate

  • Evidence of severe cognitive impairment as assessed by the Blessed Orientation-Memory-Concentration (BOMC) test weighted score

  • Untreated patients with the diagnosis of moderate-severe obstructive sleep apnea with Total Apnea-Hypopnea Index (AHI-T) of 15 events/hour of sleep

  • Subject's inability to give informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA Philadelphia Pennsylvania United States 19104

Sponsors and Collaborators

  • VA Office of Research and Development
  • University of Pennsylvania
  • University of Michigan

Investigators

  • Principal Investigator: Subhajit Chakravorty, MD, Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
VA Office of Research and Development
ClinicalTrials.gov Identifier:
NCT01987089
Other Study ID Numbers:
  • NURA-017-13S
  • 1IK2CX000855
  • 01468
First Posted:
Nov 19, 2013
Last Update Posted:
Aug 7, 2020
Last Verified:
Aug 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by VA Office of Research and Development
Additional relevant MeSH terms:

Study Results

Participant Flow

Recruitment Details 83 was the anticipated recruitment target sample and our final recruitment sample was 63
Pre-assignment Detail
Arm/Group Title Cognitive Behavioral Therapy for Insomnia (CBT-I) Quasi Desensitization Therapy (QDT)
Arm/Group Description Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. Session 1 serves as an orientation. No active treatment is delivered at this time. Sessions 2 & 3 are used to deliver the three main components of the intervention which are Sleep Restriction (SRT), Stimulus Control, and Sleep Hygiene. All but two of the remaining sessions are dedicated to the titration of total sleep time and to ensuring patient adherence. One session (session 5) entails the delivery of a specific form of cognitive therapy. The final session (session 8) is used to engage in a relapse-prevention didactic, i.e., to review first, how insomnia becomes chronic and second, the strategies that are likely to abort an extended episode of insomnia. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. This form of placebo therapy has been commonly used in prior studies investigating behavioral interventions for insomnia. The therapist presents the QDT as a means to eliminate "conditioned arousal," occurring after nocturnal arousal using 8 sessions on a weekly basis. The therapist initially helps the subject to develop a chronological 12-item hierarchy of commonly practiced activities on awakening at night, like opening eyes and clock watching. As a next step, the subject develops 6 imaginable scenes of himself/herself engaged in neutral activities like reading a newspaper. The therapist then helps the subject pair the neutral scenes with the items from the 12-item hierarchy, which is then practiced by the subject 2 hours before bedtime. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician.
Period Title: Overall Study
STARTED 31 32
COMPLETED 30 28
NOT COMPLETED 1 4

Baseline Characteristics

Arm/Group Title Cognitive Behavioral Therapy for Insomnia Quasi Desensitization Therapy Total
Arm/Group Description Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. Session 1 serves as an orientation. No active treatment is delivered at this time. Sessions 2 & 3 are used to deliver the three main components of the intervention which are Sleep Restriction (SRT), Stimulus Control, and Sleep Hygiene. All but two of the remaining sessions are dedicated to the titration of total sleep time and to ensuring patient adherence. One session (session 5) entails the delivery of a specific form of cognitive therapy. The final session (session 8) is used to engage in a relapse-prevention didactic, i.e., to review first, how insomnia becomes chronic and second, the strategies that are likely to abort an extended episode of insomnia. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. This form of placebo therapy has been commonly used in prior studies investigating behavioral interventions for insomnia. The therapist presents the QDT as a means to eliminate "conditioned arousal," occurring after nocturnal arousal using 8 sessions on a weekly basis. The therapist initially helps the subject to develop a chronological 12-item hierarchy of commonly practiced activities on awakening at night, like opening eyes and clock watching. As a next step, the subject develops 6 imaginable scenes of himself/herself engaged in neutral activities like reading a newspaper. The therapist then helps the subject pair the neutral scenes with the items from the 12-item hierarchy, which is then practiced by the subject 2 hours before bedtime. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. Total of all reporting groups
Overall Participants 31 32 63
Age (years) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [years]
51.6
(10.9)
51.5
(8.2)
51.6
(9.5)
Sex: Female, Male (Count of Participants)
Female
3
9.7%
2
6.3%
5
7.9%
Male
28
90.3%
30
93.8%
58
92.1%
Race/Ethnicity, Customized (Count of Participants)
African-American
23
74.2%
29
90.6%
52
82.5%
Caucasian
8
25.8%
3
9.4%
11
17.5%
Hispanic
1
3.2%
1
3.1%
2
3.2%
Insomnia Severity Index total score (ISI) (units on a scale) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [units on a scale]
19.7
(3.5)
19.0
(3.7)
19.3
(3.6)
Sleep Onset Latency (SOL, sleep diary) (minutes) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [minutes]
51.6
(41.4)
49.3
(34.0)
50.5
(37.7)
Wake After Sleep Onset (WASO, sleep diary) (minutes) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [minutes]
44.6
(30.0)
28.6
(25.5)
36.7
(28.8)
Total Sleep Time (TST, sleep diary) (minutes) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [minutes]
317.0
(90.8)
345.1
(99.5)
330.8
(95.5)
Percent Days Abstinent (PDA, last 90 days, at screening) (Percent of Days Abstinent) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [Percent of Days Abstinent]
38.3
(36.0)
26.9
(29.2)
32.5
(32.9)
Drinks per day (DrPDay, last 90 days, at screening) (Number of Drinks Per Day) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [Number of Drinks Per Day]
9.1
(9.2)
8.8
(7.1)
8.9
(8.1)
Penn Alcohol Craving Scale total score (PACS) (units on a scale) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [units on a scale]
10.8
(7.5)
8.2
(7.0)
9.5
(7.3)
Days Abstinent from Alcohol before Treatment (Abs) (Number of Days) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [Number of Days]
86.8
(103.3)
142.6
(111.6)
115.2
(110.4)
Physical Composite Score (PCS, SF-12 scale) (units on a scale) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [units on a scale]
42.7
(4.6)
40.4
(5.3)
41.7
(5.0)
Mental Composite Score (MCS, SF-12 scale) (units on a scale) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [units on a scale]
44.4
(7.5)
43.1
(6.4)
43.9
(6.9)
Beck Depression Inventory total score (units on a scale) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [units on a scale]
19.7
(12.4)
17.2
(10.7)
18.5
(11.6)
State Trait Anxiety Inventory - trait subscale (STAI-trait) (units on a scale) [Mean (Standard Deviation) ]
Mean (Standard Deviation) [units on a scale]
45.0
(5.9)
46.3
(6.0)
45.6
(5.9)

Outcome Measures

1. Primary Outcome
Title Change in Insomnia Severity Index - Total Score
Description Insomnia Severity Index (ISI): This 7-item (0-4 Likert scales) measure yields a total score of 28. The norms for the scale are as follows: 0-7 represents no clinically significant insomnia; 8-14 represents sub threshold insomnia; 15-21 represents clinical insomnia (moderate severity); 21-28 represents clinical insomnia (severe). The scale provides a measure of severity of insomnia (overall), a measure of insomnia subtype, a measure of the diurnal effects of insomnia, and a measure of sleep "satisfaction". The ISI will be completed at baseline and for all the subsequent study-related visits.
Time Frame 8 weeks, 3 months post-treatment, and 6 months post-treatment

Outcome Measure Data

Analysis Population Description
All subjects randomized into either treatment arm and received had 1 or more treatment sessions.
Arm/Group Title Cognitive Behavioral Therapy for Insomnia (CBT-I) Quasi Desensitization Therapy (QDT)
Arm/Group Description Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. Session 1 serves as an orientation. No active treatment is delivered at this time. Sessions 2 & 3 are used to deliver the three main components of the intervention which are Sleep Restriction (SRT), Stimulus Control, and Sleep Hygiene. All but two of the remaining sessions are dedicated to the titration of total sleep time and to ensuring patient adherence. One session (session 5) entails the delivery of a specific form of cognitive therapy. The final session (session 8) is used to engage in a relapse-prevention didactic, i.e., to review first, how insomnia becomes chronic and second, the strategies that are likely to abort an extended episode of insomnia. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. This form of placebo therapy has been commonly used in prior studies investigating behavioral interventions for insomnia. The therapist presents the QDT as a means to eliminate "conditioned arousal," occurring after nocturnal arousal using 8 sessions on a weekly basis. The therapist initially helps the subject to develop a chronological 12-item hierarchy of commonly practiced activities on awakening at night, like opening eyes and clock watching. As a next step, the subject develops 6 imaginable scenes of himself/herself engaged in neutral activities like reading a newspaper. The therapist then helps the subject pair the neutral scenes with the items from the 12-item hierarchy, which is then practiced by the subject 2 hours before bedtime. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician.
Measure Participants 31 32
Change at week 8 (Vs baseline)
-10.71
-8.84
Change at 3 mo post-treatment F/U (Vs baseline)
-8.51
-9.30
Change at 6 mo post-treatment F/U (Vs baseline)
-6.89
-7.29
2. Primary Outcome
Title Change in Percent Days Abstinent (PDA) on the Time Line Follow Back Measure
Description Time Line Follow Back measure (TLFB): The TLFB provides assessment of drinking using a calendar format for the number of standard alcoholic beverages consumed per day. A standard drink, as defined by the National Institutes of Health, is 12 oz of regular beer, 5 oz of regular wine, or 1.5 oz of distilled spirits (e.g. whiskey). Numerous indices may be derived from the TLFB, such as the Percent Days Abstinent (PDA) proposed in this study. The PDA is derived as the percentage of days an individual reports being abstinent from alcohol within a given assessment time period.
Time Frame 8 weeks, 3 months post-treatment and 6-months post-treatment

Outcome Measure Data

Analysis Population Description
All subjects randomized into either treatment arm and received had 1 or more treatment sessions.
Arm/Group Title Cognitive Behavioral Therapy for Insomnia (CBT-I) Quasi Desensitization Therapy (QDT)
Arm/Group Description Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. Session 1 serves as an orientation. No active treatment is delivered at this time. Sessions 2 & 3 are used to deliver the three main components of the intervention which are Sleep Restriction (SRT), Stimulus Control, and Sleep Hygiene. All but two of the remaining sessions are dedicated to the titration of total sleep time and to ensuring patient adherence. One session (session 5) entails the delivery of a specific form of cognitive therapy. The final session (session 8) is used to engage in a relapse-prevention didactic, i.e., to review first, how insomnia becomes chronic and second, the strategies that are likely to abort an extended episode of insomnia. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. This form of placebo therapy has been commonly used in prior studies investigating behavioral interventions for insomnia. The therapist presents the QDT as a means to eliminate "conditioned arousal," occurring after nocturnal arousal using 8 sessions on a weekly basis. The therapist initially helps the subject to develop a chronological 12-item hierarchy of commonly practiced activities on awakening at night, like opening eyes and clock watching. As a next step, the subject develops 6 imaginable scenes of himself/herself engaged in neutral activities like reading a newspaper. The therapist then helps the subject pair the neutral scenes with the items from the 12-item hierarchy, which is then practiced by the subject 2 hours before bedtime. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician.
Measure Participants 31 32
Change at week 8 (Vs baseline)
0.56
0.67
Change at 3 mo post-treatment F/U (Vs baseline)
0.51
0.61
Change at 6 mo post-treatment F/U (Vs baseline)
0.48
0.62
3. Other Pre-specified Outcome
Title Change in PCS From the Short Form - 12 Item (SF-12) Measure
Description The Physical Component Summary (PCS) scale has a range from 0 (indicating the lowest level of health) to 100 (indicating the best level of health).
Time Frame 8 weeks, 3 months post-treatment, and 6 months post-treatment

Outcome Measure Data

Analysis Population Description
All subjects randomized into either treatment arm and received had 1 or more treatment sessions.
Arm/Group Title Cognitive Behavioral Therapy for Insomnia (CBT-I) Quasi Desensitization Therapy (QDT)
Arm/Group Description Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. Session 1 serves as an orientation. No active treatment is delivered at this time. Sessions 2 & 3 are used to deliver the three main components of the intervention which are Sleep Restriction (SRT), Stimulus Control, and Sleep Hygiene. All but two of the remaining sessions are dedicated to the titration of total sleep time and to ensuring patient adherence. One session (session 5) entails the delivery of a specific form of cognitive therapy. The final session (session 8) is used to engage in a relapse-prevention didactic, i.e., to review first, how insomnia becomes chronic and second, the strategies that are likely to abort an extended episode of insomnia. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. This form of placebo therapy has been commonly used in prior studies investigating behavioral interventions for insomnia. The therapist presents the QDT as a means to eliminate "conditioned arousal," occurring after nocturnal arousal using 8 sessions on a weekly basis. The therapist initially helps the subject to develop a chronological 12-item hierarchy of commonly practiced activities on awakening at night, like opening eyes and clock watching. As a next step, the subject develops 6 imaginable scenes of himself/herself engaged in neutral activities like reading a newspaper. The therapist then helps the subject pair the neutral scenes with the items from the 12-item hierarchy, which is then practiced by the subject 2 hours before bedtime. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician.
Measure Participants 31 32
Change at week 8 (Vs baseline)
-1.00
0.48
Change at 3 mo post-treatment F/U (Vs baseline)
-1.69
0.54
Change at 6 mo post-treatment F/U (Vs baseline)
-1.18
-0.25
4. Other Pre-specified Outcome
Title Change in MCS From the Short Form - 12 Item (SF-12) Measure
Description The Mental Component Summary (MCS) scale has a range from 0 (indicating the lowest level of health) to 100 (indicating the best level of health).
Time Frame 8 weeks, 3 months post-treatment, and 6 months post-treatment

Outcome Measure Data

Analysis Population Description
All subjects randomized into either treatment arm and received had 1 or more treatment sessions.
Arm/Group Title Cognitive Behavioral Therapy for Insomnia (CBT-I) Quasi Desensitization Therapy (QDT)
Arm/Group Description Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. Session 1 serves as an orientation. No active treatment is delivered at this time. Sessions 2 & 3 are used to deliver the three main components of the intervention which are Sleep Restriction (SRT), Stimulus Control, and Sleep Hygiene. All but two of the remaining sessions are dedicated to the titration of total sleep time and to ensuring patient adherence. One session (session 5) entails the delivery of a specific form of cognitive therapy. The final session (session 8) is used to engage in a relapse-prevention didactic, i.e., to review first, how insomnia becomes chronic and second, the strategies that are likely to abort an extended episode of insomnia. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. This form of placebo therapy has been commonly used in prior studies investigating behavioral interventions for insomnia. The therapist presents the QDT as a means to eliminate "conditioned arousal," occurring after nocturnal arousal using 8 sessions on a weekly basis. The therapist initially helps the subject to develop a chronological 12-item hierarchy of commonly practiced activities on awakening at night, like opening eyes and clock watching. As a next step, the subject develops 6 imaginable scenes of himself/herself engaged in neutral activities like reading a newspaper. The therapist then helps the subject pair the neutral scenes with the items from the 12-item hierarchy, which is then practiced by the subject 2 hours before bedtime. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician.
Measure Participants 31 32
Change at week 8 (Vs baseline)
-3.06
-1.90
Change at 3 mo post-treatment F/U (Vs baseline)
-2.60
1.12
Change at 6 mo post-treatment F/U (Vs baseline)
-2.07
0.89

Adverse Events

Time Frame 9 months
Adverse Event Reporting Description This a behavioral treatment intervention study.
Arm/Group Title Cognitive Behavioral Therapy for Insomnia (CBT-I) Quasi Desensitization Therapy (QDT)
Arm/Group Description Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. Session 1 serves as an orientation. No active treatment is delivered at this time. Sessions 2 & 3 are used to deliver the three main components of the intervention which are Sleep Restriction (SRT), Stimulus Control, and Sleep Hygiene. All but two of the remaining sessions are dedicated to the titration of total sleep time and to ensuring patient adherence. One session (session 5) entails the delivery of a specific form of cognitive therapy. The final session (session 8) is used to engage in a relapse-prevention didactic, i.e., to review first, how insomnia becomes chronic and second, the strategies that are likely to abort an extended episode of insomnia. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician. This form of placebo therapy has been commonly used in prior studies investigating behavioral interventions for insomnia. The therapist presents the QDT as a means to eliminate "conditioned arousal," occurring after nocturnal arousal using 8 sessions on a weekly basis. The therapist initially helps the subject to develop a chronological 12-item hierarchy of commonly practiced activities on awakening at night, like opening eyes and clock watching. As a next step, the subject develops 6 imaginable scenes of himself/herself engaged in neutral activities like reading a newspaper. The therapist then helps the subject pair the neutral scenes with the items from the 12-item hierarchy, which is then practiced by the subject 2 hours before bedtime. Cognitive Behavioral Therapy for Insomnia (CBT-I): Eight Session CBT-I: Cognitive Behavioral therapy is conducted in 8 individual sessions with the study clinician.
All Cause Mortality
Cognitive Behavioral Therapy for Insomnia (CBT-I) Quasi Desensitization Therapy (QDT)
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/31 (0%) 0/32 (0%)
Serious Adverse Events
Cognitive Behavioral Therapy for Insomnia (CBT-I) Quasi Desensitization Therapy (QDT)
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 7/31 (22.6%) 3/32 (9.4%)
Gastrointestinal disorders
Abdominal Pain 1/31 (3.2%) 0/32 (0%)
Nervous system disorders
Cerebrovascular Accident (CVA) 0/31 (0%) 1/32 (3.1%)
Alcohol detoxification 4/31 (12.9%) 2/32 (6.3%)
Residential Psychiatric Treatment 1/31 (3.2%) 0/32 (0%)
Respiratory, thoracic and mediastinal disorders
Pneumonia 1/31 (3.2%) 0/32 (0%)
Other (Not Including Serious) Adverse Events
Cognitive Behavioral Therapy for Insomnia (CBT-I) Quasi Desensitization Therapy (QDT)
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/31 (0%) 0/32 (0%)

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

All Principal Investigators ARE employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Results Point of Contact

Name/Title Subhajit Chakravorty
Organization Crescenz VA Medical Center
Phone (215)-823-5800
Email Subhajit.Chakravorty@va.gov
Responsible Party:
VA Office of Research and Development
ClinicalTrials.gov Identifier:
NCT01987089
Other Study ID Numbers:
  • NURA-017-13S
  • 1IK2CX000855
  • 01468
First Posted:
Nov 19, 2013
Last Update Posted:
Aug 7, 2020
Last Verified:
Aug 1, 2020