Chronic Insomnia Clinical Trial
— NEXPERTSANTEOfficial title:
Pilot Study Evaluating the Efficacy of the Management of an Online Program of Cognitive Behavioral Therapy for Primary Insomnia
NCT number | NCT02539862 |
Other study ID # | 9454 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 9, 2015 |
Est. completion date | May 2016 |
Verified date | May 2018 |
Source | University Hospital, Montpellier |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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).
Status | Completed |
Enrollment | 46 |
Est. completion date | May 2016 |
Est. primary completion date | May 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 65 Years |
Eligibility |
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 |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Montpellier | Institut National de la Santé Et de la Recherche Médicale, France |
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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). | 100 days | |
Secondary | sleep efficiency | duration of of sleep time compared to the time window passed to bed | 100 days | |
Secondary | Sleep latency | collection of data with actiwatch2 sensor | 100 days | |
Secondary | duration of night wakings | collection of data with actiwatch2 sensor | 100 days | |
Secondary | total sleep time | The total sleep time measured by sleep diary and actometer (Actiwatch 2 Sleep). | 100 days | |
Secondary | Sleep quality | sleepiness score assessed by a specific questionnaire | 100 days | |
Secondary | quantity of hypnotic treatment | number of hypnotic which will be consume by patient | 100 days | |
Secondary | adherence to CBT-I program online | the number of steps performed in the program, and the weekly frequency of connection. | 100 days |
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