Better Sleep in Psychiatric Care - Depression, Anxiety and Trauma, Pilot Study

Sponsor
Karolinska Institutet (Other)
Overall Status
Completed
CT.gov ID
NCT05379244
Collaborator
Region Stockholm (Other)
18
1
1
13
1.4

Study Details

Study Description

Brief Summary

Between 50-80 percent of patients in psychiatry have insomnia-type sleep problems. In addition to reduced quality of life and impaired function, sleep problems can aggravate other psychiatric problems and increase the risk of relapse into, for example, depression. According to international guidelines, cognitive behavioral therapy for insomnia (CBT-i) should be used as the first choice for treatment of insomnia. In practice, however, it is very uncommon for psychiatric patients to be offered CBT-i, instead most are treated with sleep medications. There is also a lack of research studies evaluating CBT-i in regular clinical practice.

This pilot study investigated the feasibility of a group treatment with CBT-i at a psychiatric outpatient clinic in Stockholm for patients with depression, bipolar disorder II, anxiety syndrome and PTSD. Changes in symptoms of insomnia, depression, and anxiety after treatment were also investigated.

Patients with self-perceived sleep problems were offered a six-session group treatment based on CBT-i. The primary outcome was clinical feasibility, defined as: the influx of patients sufficient to start at least one group per semester (at least 8 patients); at least half of included patients participate in the first session; patients participate in at least half of the sessions; less than half of the patients drop out of treatment; group leaders find the treatment manual credible, easy to use and want to continue working with it after the study is completed.

Secondary outcomes were changes in insomnia symptoms, and changes in symptoms of depression and anxiety.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: CBT-i
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
18 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
Single Group Assignment Pragmatic, within-group pilot studySingle Group Assignment Pragmatic, within-group pilot study
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Better Sleep in Psychiatric Care - Clinical Feasibility and Preliminary Effects of CBT for Insomnia in a Mixed Psychiatric Sample at an Outpatient Clinic
Actual Study Start Date :
Jan 1, 2019
Actual Primary Completion Date :
Oct 1, 2019
Actual Study Completion Date :
Jan 31, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: CBT-i

Cognitive Behavioral Therapy for insomnia adjusted for patients with mixed psychiatric disorders

Behavioral: CBT-i
Behavioral intervention based on Cognitive Behavioral Therapy for insomnia, adjusted for psychiatric patients with anxiety disorders, affective disorders and trauma

Outcome Measures

Primary Outcome Measures

  1. Number of participants registering to participate in the treatment [Screening]

    Influx of patients should be sufficient to start at least one group per semester (at least 8 patients)

  2. Number of included participants attending the first treatment session [First session (1 week)]

    At least half of included patients should attend the first treatment session

  3. Number sessions attended by the participants [Post-treatment (6 weeks)]

    Average number of sessions attended should be no less than 3

  4. Number of participants dropping out of treatment [Post-treatment (6 weeks)]

    Less than half of the patients should drop out of treatment

  5. Qualitative measure of group leaders' perception of the manual [Post-treatment (6 weeks)]

    Group leaders should find the treatment manual credible and easy to use, and be willing to continue using the treatment manual after the study is completed

Secondary Outcome Measures

  1. Insomnia Severity Index [Post-treatment (6 weeks), Three-month follow-up (21 weeks)]

    7-item self-reported measure of insomnia severity, 0-28 points, lower is better.

  2. Patient health questionnaire (PHQ-9) [Post-treatment (6 weeks), Three-month follow-up (21 weeks)]

    9-item depression inventory, 0-27 points, lower is better

  3. Generalized Anxiety Disorder Assessment (GAD-7) [Post-treatment (6 weeks), Three-month follow-up (21 weeks)]

    7-item anxiety inventory, 0-21 points, lower is better

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Being a patient at a specialist outpatient clinic treating these patient groups

  • Insomnia disorder or sleep problems of insomnia type

  • Over 10 points on the Insomnia Severity Index (ISI)

  • Adequate skills in written and spoken Swedish

  • No practical barriers to participate in the group treatment

Exclusion Criteria:
  • night shift work

  • ongoing alcohol or drug abuse that required treatment at a specialised unit

Contacts and Locations

Locations

Site City State Country Postal Code
1 Program for Anxiety and Affective disorders, Stockholm Southwest Psychiatry Stockholm Sweden 141 86

Sponsors and Collaborators

  • Karolinska Institutet
  • Region Stockholm

Investigators

  • Principal Investigator: Susanna Jernelöv, PhD, Karolinska Institutet

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Susanna Jernelöv, Associate Professor, Karolinska Institutet
ClinicalTrials.gov Identifier:
NCT05379244
Other Study ID Numbers:
  • 2018/80-31/1a
First Posted:
May 18, 2022
Last Update Posted:
Jun 10, 2022
Last Verified:
Jun 1, 2022
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
Keywords provided by Susanna Jernelöv, Associate Professor, Karolinska Institutet
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 10, 2022