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"Get up" - The Sleep Study in Oppegard (Stå Opp)

Primary Purpose

Sleep Initiation and Maintenance Disorders

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Sleep Restriction Therapy/Stimulus Control
Discussions about adverse cognitions about sleep
Psychoeducative advice about how to improve sleep
Sponsored by
Norwegian Institute of Public Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sleep Initiation and Maintenance Disorders focused on measuring Insomnia, Cognitive behavioral treatment for insomnia (CBT-I)

Eligibility Criteria

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

Inclusion Criteria:

  • persons above the age of 18
  • living in the municipalities of Oppegård and Ski
  • fits the criteria for moderate or severe clinical insomnia, as measured by Insomnia Severity Index (Bastien C. H., Valliéres A., Morin C. M., 2001)

Exclusion Criteria:

  • bipolar disorder
  • epilepsy
  • severe depressive episode
  • psychosis disorders
  • somatic sleep disorders (untreated sleep apnea, restless leg syndrome, narcolepsy, and sleepwalking)
  • persons with a high risk of falling at home
  • persons handling heavy machinery
  • severe personality disorders

Sites / Locations

  • Oppegård kommune

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Treatment groups spring (1,2)

Waiting list - Treatment groups fall

Psychoeducative course in Nesodden

Arm Description

Seven sessions CBT-I treatment for two different groups of eight participants (n=16) Interventions: Sleep restriction/Stimulus Control Discussion of adverse cognitions about sleep

This group (n=22) receives no treatment during the spring and summer, and is measured three times as a waiting list control in this period of time. The same group will receive treatment i three different groups during sept/oct. Interventions: Sleep restriction/Stimulus Control Discussion of adverse cognitions about sleep

This group (expected to be n=16) will receive a four session psychoeducative learning based course on how to manage insomnia Interventions: Psychoeducative advice to improve sleep

Outcomes

Primary Outcome Measures

Insomnia Severity Index
Reduction in score on the Insomnia Severity Index

Secondary Outcome Measures

Generalized Anxiety Disorder 7-item Scale (GAD-7)
Reduction in anxiety symptoms by the end of the treatment period
The Patient Health Questionnaire (PHQ-9)
Reduction in symptoms of depression by the end of the treatment period

Full Information

First Posted
June 2, 2017
Last Updated
March 12, 2019
Sponsor
Norwegian Institute of Public Health
Collaborators
University of Oslo
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1. Study Identification

Unique Protocol Identification Number
NCT03177967
Brief Title
"Get up" - The Sleep Study in Oppegard
Acronym
Stå Opp
Official Title
"Get up" - The Sleep Study in Oppegard (Stå Opp - Søvnstudien i Oppegård)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
April 24, 2017 (Actual)
Primary Completion Date
December 1, 2017 (Actual)
Study Completion Date
December 1, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Norwegian Institute of Public Health
Collaborators
University of Oslo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A randomized, controlled study to examine the effect of group treatment for insomnia (CBT-I) in an outpatient clinic compared with waiting list and treatment-as-usual (sleep-hygiene based educational course)
Detailed Description
Insomnia is a large public health concern with latest reports pointing to almost 15 % of the population in Norway having insomnia (Pallesen, Sivertsen, Nordhus, & Bjorvatn, 2014). At the same time there is a scientific consensus about how to best treat insomnia (CBT-I), and it is empirically proven that this is quite effective treatment (Okajima, Komada & Inoue, 2011). We therefore want to conduct a study to examine if CBT-I treatment in an public outpatient clinic is effective compared with waiting list and a psychoeducational course. The design is a randomized controlled study with three different conditions (CBT-I versus waiting list versus TAU) that will be compared over time. We will use an A-B-design which can effectively compare the different conditions in the study. We have recruited a total of 62 patients, and completed a individual session with each of these individuals resulting in a total admission of 38 participants in the study. The remaining 24 patients either didn't fit the selection criteria, or we were unable to get in touch with them to agree on an appointment. Of the 38 participants enrolled in the study, 16 will get CBT-I, Group based treatment during May and June of 2017 (a total of seven sessions over nine weeks), and the remaining 22 will get the same treatment in September and October 2017. The maximum number of patients per group is eight (8) and we randomized whether participants got assigned to treatment in May/June or September/October. We measure all participants at the individual pre-screening (T1), Treatment Group 1 and 2 gets treatment in May and June and will be measured in every other treatment session (2,4,6 and 7) From now on called (T2, T3, T4, T5). Treatment Group 3,4 and 5 (all getting treatment i September/October) is measured at T2 and T5. T1 was conducted during the last week of April and T5 is towards the end of June 2017. Treatment Group 3, 4 and 5 will start their treatment and be measured at session 2 (T6) in mid-September, and Treatment Group 1 and 2 will also be measured at this point. Treatment Group 3, 4 and 5 will then be measured at treatment session 4,6 and 7, just like treatment Group 1 and 2 was during their treatment. (From now on T7, T8, T9). Treatment Groups 1 and 2 will also be measured at T9. The treatment-as-usual condition is conducted in Nesodden kommune, and it is a psychoeducative, learning based course. This course consists of 4 sessions, and the participants is measured at session 1,3 and 4 in addition to a 6 months follow-up measure. They also get measured at pre-screening. We expect about 16 participants to complete this course.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Initiation and Maintenance Disorders
Keywords
Insomnia, Cognitive behavioral treatment for insomnia (CBT-I)

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Treatment groups spring (1,2)
Arm Type
Experimental
Arm Description
Seven sessions CBT-I treatment for two different groups of eight participants (n=16) Interventions: Sleep restriction/Stimulus Control Discussion of adverse cognitions about sleep
Arm Title
Waiting list - Treatment groups fall
Arm Type
Experimental
Arm Description
This group (n=22) receives no treatment during the spring and summer, and is measured three times as a waiting list control in this period of time. The same group will receive treatment i three different groups during sept/oct. Interventions: Sleep restriction/Stimulus Control Discussion of adverse cognitions about sleep
Arm Title
Psychoeducative course in Nesodden
Arm Type
Active Comparator
Arm Description
This group (expected to be n=16) will receive a four session psychoeducative learning based course on how to manage insomnia Interventions: Psychoeducative advice to improve sleep
Intervention Type
Behavioral
Intervention Name(s)
Sleep Restriction Therapy/Stimulus Control
Intervention Description
Sleep Restriction Therapy focuses on forcing your available sleep time into a fixed window. The sleeper sets a bedtime and wake-up time and sticks to those times closely. The time allocated for being allowed in bed is determined from an estimate of how long the patient in average has been sleeping during the night, in the week before treatment. The goal is to have the patient sleeping the entire time he or she is in bed by making this period so restricted that the patient has no chance of sleeping enough. Once this goal is achieved, the time allocated for bed can be slowly increased, for example by 15 minutes at a time. After enough iterations, an equilibrium is achieved that the patient can keep maintaining after treatment has completed.
Intervention Type
Other
Intervention Name(s)
Discussions about adverse cognitions about sleep
Intervention Description
Group discussions about insomnia, CBT-i treatment and it's effects
Intervention Type
Other
Intervention Name(s)
Psychoeducative advice about how to improve sleep
Intervention Description
Learning about sleep and sleep hygiene tips. It also includes learning about stimulus control and sleep restriction.
Primary Outcome Measure Information:
Title
Insomnia Severity Index
Description
Reduction in score on the Insomnia Severity Index
Time Frame
We expect the decline in insomnia symptoms to start by session four (late may, 2017), and continue through session six (medio june, 2017) and seven (late june, 2017), and to be maintained at six-months follow up (november, 2017).
Secondary Outcome Measure Information:
Title
Generalized Anxiety Disorder 7-item Scale (GAD-7)
Description
Reduction in anxiety symptoms by the end of the treatment period
Time Frame
We expect the decline in anxiety symptoms to start declining by session four (late may, 2017), and to be maintained at six-months follow up (november, 2017).
Title
The Patient Health Questionnaire (PHQ-9)
Description
Reduction in symptoms of depression by the end of the treatment period
Time Frame
We expect the decline in symptoms of depression to start declining by session four (late may, 2017), and to be maintained at six-months follow up (november, 2017).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: persons above the age of 18 living in the municipalities of Oppegård and Ski fits the criteria for moderate or severe clinical insomnia, as measured by Insomnia Severity Index (Bastien C. H., Valliéres A., Morin C. M., 2001) Exclusion Criteria: bipolar disorder epilepsy severe depressive episode psychosis disorders somatic sleep disorders (untreated sleep apnea, restless leg syndrome, narcolepsy, and sleepwalking) persons with a high risk of falling at home persons handling heavy machinery severe personality disorders
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Knut Inge Klepp, PhD
Organizational Affiliation
Executive director
Official's Role
Study Chair
Facility Information:
Facility Name
Oppegård kommune
City
Kolbotn
State/Province
Akershus
ZIP/Postal Code
1410
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
Citation
Okajima, I., Komada, Y. and Inoue, Y. (2011), A meta-analysis on the treatment effectiveness of cognitive behavioral therapy for primary insomnia. Sleep and Biological Rhythms, 9: 24-34. doi:10.1111/j.1479-8425.2010.00481.x
Results Reference
background
PubMed Identifier
24382513
Citation
Pallesen S, Sivertsen B, Nordhus IH, Bjorvatn B. A 10-year trend of insomnia prevalence in the adult Norwegian population. Sleep Med. 2014 Feb;15(2):173-9. doi: 10.1016/j.sleep.2013.10.009. Epub 2013 Dec 1.
Results Reference
background
PubMed Identifier
21886353
Citation
Kessler RC, Berglund PA, Coulouvrat C, Hajak G, Roth T, Shahly V, Shillington AC, Stephenson JJ, Walsh JK. Insomnia and the performance of US workers: results from the America insomnia survey. Sleep. 2011 Sep 1;34(9):1161-71. doi: 10.5665/SLEEP.1230. Erratum In: Sleep. 2011;34(11):1608. Sleep. 2012 Jun 1;35(6):725.
Results Reference
background
PubMed Identifier
22879427
Citation
Sivertsen B, Salo P, Mykletun A, Hysing M, Pallesen S, Krokstad S, Nordhus IH, Overland S. The bidirectional association between depression and insomnia: the HUNT study. Psychosom Med. 2012 Sep;74(7):758-65. doi: 10.1097/PSY.0b013e3182648619. Epub 2012 Aug 9.
Results Reference
background
PubMed Identifier
16448292
Citation
Irwin MR, Cole JC, Nicassio PM. Comparative meta-analysis of behavioral interventions for insomnia and their efficacy in middle-aged adults and in older adults 55+ years of age. Health Psychol. 2006 Jan;25(1):3-14. doi: 10.1037/0278-6133.25.1.3.
Results Reference
background
PubMed Identifier
26054060
Citation
Trauer JM, Qian MY, Doyle JS, Rajaratnam SM, Cunnington D. Cognitive Behavioral Therapy for Chronic Insomnia: A Systematic Review and Meta-analysis. Ann Intern Med. 2015 Aug 4;163(3):191-204. doi: 10.7326/M14-2841.
Results Reference
background
PubMed Identifier
26212846
Citation
Falloon K, Elley CR, Fernando A 3rd, Lee AC, Arroll B. Simplified sleep restriction for insomnia in general practice: a randomised controlled trial. Br J Gen Pract. 2015 Aug;65(637):e508-15. doi: 10.3399/bjgp15X686137.
Results Reference
background
Available IPD and Supporting Information:
Available IPD/Information Type
Study Protocol
Available IPD/Information URL
https://www.oppegard.kommune.no/helse/psykisk-helsetjeneste-
Available IPD/Information Comments
The study protocol is unfortunately only available in Norwegian at the time being.

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"Get up" - The Sleep Study in Oppegard

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