Evaluating the Efficacy of the Management of an Online Program of Cognitive Behavioral Therapy for Primary Insomnia (NEXPERTSANTE)
Primary Purpose
Chronic Insomnia
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
cognitive behavioral therapy online
psychoeducation
Sponsored by
About this trial
This is an interventional supportive care trial for Chronic Insomnia focused on measuring Insomnia, behavioral and cognitive therapies
Eligibility Criteria
Inclusion Criteria:
- age between 20 and 65
- disorder diagnosis of chronic insomnia (according to Diagnostic and Statistical Manual-5)
- sleep efficiency <80%
- Index severe insomnia: ISI> 14/28
- have a computer at home
- Practicing internet regularly in everyday life
- have a personal email address
Exclusion Criteria:
- Clinically suffer from insomnia comorbid linked to other sleep disorders
- Presenting an unbalanced psychiatric disorder
- Have Score Beck Depression Inventory (BDI-II) >29
- Have neurological disorders
- Have severe medical conditions that can affect the quality of sleep
- Have Hypnotic, Anxiolytic, antidepressants Treatment > 2
- Have antipsychotics, opioids, anticonvulsants, anti-parkinson treatment
- Having a disorder of substance use (alcohol, drugs) in the last 6 months
- Having undertaken a meridian trance journey (± 3H) in the preceding month or during the study period
- Already be treated with CBT-I
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
cognitive behavioral therapy online
no cognitive behavioral therapy online
Arm Description
patients receive cognitive behavioral therapy via an online program
patients receive psychoeducation by a doctor
Outcomes
Primary Outcome Measures
insomnia severity measured
The primary endpoint will focus on the severity of insomnia measured by the Index severe insomnia (ISI) at the end of the last session of CBT (3 months) between the 2 groups of patients (CBT-I online and psychoeducation).
Secondary Outcome Measures
sleep efficiency
duration of of sleep time compared to the time window passed to bed
Sleep latency
collection of data with actiwatch2 sensor
duration of night wakings
collection of data with actiwatch2 sensor
total sleep time
The total sleep time measured by sleep diary and actometer (Actiwatch 2 Sleep).
Sleep quality
sleepiness score assessed by a specific questionnaire
quantity of hypnotic treatment
number of hypnotic which will be consume by patient
adherence to CBT-I program online
the number of steps performed in the program, and the weekly frequency of connection.
Full Information
NCT ID
NCT02539862
First Posted
July 24, 2015
Last Updated
May 9, 2018
Sponsor
University Hospital, Montpellier
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France
1. Study Identification
Unique Protocol Identification Number
NCT02539862
Brief Title
Evaluating the Efficacy of the Management of an Online Program of Cognitive Behavioral Therapy for Primary Insomnia
Acronym
NEXPERTSANTE
Official Title
Pilot Study Evaluating the Efficacy of the Management of an Online Program of Cognitive Behavioral Therapy for Primary Insomnia
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
July 9, 2015 (Actual)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
May 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the effectiveness of the management of chronic primary insomnia patients by a computer program guidance of behavioral and cognitive therapies for insomnia (BCT-I).
Detailed Description
Chronic insomnia is a common sleep disorder (prevalence = 10%) and a risk identified on the physical and mental health. Currently, the treatment involves the prescription of drug treatments by general practitioners, which may be unsuitable for the medium term. It is better to turn to Behavioral and Cognitive Therapies for Insomnia (BCT-I) in the case of primary chronic insomnia. The objective of this study is to evaluate the effectiveness of a computer program guidance BCT-I in patients with chronic primary insomnia. This biomedical research psychotherapeutic assessment will be randomized, controlled versus psychoeducation and conducted in 46 patients with chronic primary insomnia (defined according to Diagnostic and Statistical Manual-5) for which a supported by BCT-I is indicated.
The 46 patients will be randomized into two groups. The subjects in Group 1 will be supported by BCT-I online. And the subjects in group 2 will receive psychoeducation. All patients will be followed by the research team for three months, during which 3 visits (V0 = pre-selection; V1 = visit of randomization and start of the program; V2 = 3 months follow-up visit and end of the study) will be performed in the University Hospital Sleep Disorder Unit of Montpellier. Patients in Group 1 will conduct BCT-I online at home therapy. Patients in group 2 will receive a structured 45-minute session information insomnia (psychoeducation = work performed daily by clinicians in charge of insomnia problems) to the visit 1. All patients in the study will be equipped 2 sensors for the registration of sleep data.
The primary endpoint will be based on the severity of insomnia measured by the ISI after the last online psychotherapy session (3 months) between the 2 groups of patients (BCT-I online and without treatment - psychoeducation ). The analyse efficacity to be conducted by intention to treat.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Insomnia
Keywords
Insomnia, behavioral and cognitive therapies
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
46 (Actual)
8. Arms, Groups, and Interventions
Arm Title
cognitive behavioral therapy online
Arm Type
Experimental
Arm Description
patients receive cognitive behavioral therapy via an online program
Arm Title
no cognitive behavioral therapy online
Arm Type
Other
Arm Description
patients receive psychoeducation by a doctor
Intervention Type
Other
Intervention Name(s)
cognitive behavioral therapy online
Intervention Description
The cognitive behavioral therapy online program is delivered through an accessible web application on a web browser with a personal password
Intervention Type
Other
Intervention Name(s)
psychoeducation
Intervention Description
the psychoeducation is delivered by a doctor
Primary Outcome Measure Information:
Title
insomnia severity measured
Description
The primary endpoint will focus on the severity of insomnia measured by the Index severe insomnia (ISI) at the end of the last session of CBT (3 months) between the 2 groups of patients (CBT-I online and psychoeducation).
Time Frame
100 days
Secondary Outcome Measure Information:
Title
sleep efficiency
Description
duration of of sleep time compared to the time window passed to bed
Time Frame
100 days
Title
Sleep latency
Description
collection of data with actiwatch2 sensor
Time Frame
100 days
Title
duration of night wakings
Description
collection of data with actiwatch2 sensor
Time Frame
100 days
Title
total sleep time
Description
The total sleep time measured by sleep diary and actometer (Actiwatch 2 Sleep).
Time Frame
100 days
Title
Sleep quality
Description
sleepiness score assessed by a specific questionnaire
Time Frame
100 days
Title
quantity of hypnotic treatment
Description
number of hypnotic which will be consume by patient
Time Frame
100 days
Title
adherence to CBT-I program online
Description
the number of steps performed in the program, and the weekly frequency of connection.
Time Frame
100 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age between 20 and 65
disorder diagnosis of chronic insomnia (according to Diagnostic and Statistical Manual-5)
sleep efficiency <80%
Index severe insomnia: ISI> 14/28
have a computer at home
Practicing internet regularly in everyday life
have a personal email address
Exclusion Criteria:
Clinically suffer from insomnia comorbid linked to other sleep disorders
Presenting an unbalanced psychiatric disorder
Have Score Beck Depression Inventory (BDI-II) >29
Have neurological disorders
Have severe medical conditions that can affect the quality of sleep
Have Hypnotic, Anxiolytic, antidepressants Treatment > 2
Have antipsychotics, opioids, anticonvulsants, anti-parkinson treatment
Having a disorder of substance use (alcohol, drugs) in the last 6 months
Having undertaken a meridian trance journey (± 3H) in the preceding month or during the study period
Already be treated with CBT-I
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dauvilliers Yves
Organizational Affiliation
Unit of sleep disorders
Official's Role
Principal Investigator
12. IPD Sharing Statement
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Evaluating the Efficacy of the Management of an Online Program of Cognitive Behavioral Therapy for Primary Insomnia
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