Insomnia Clinical Trial
Official title:
Implementation of Internet-based Cognitive Behaviour Therapy for Adolescents With Co-morbid Insomnia
Verified date | April 2021 |
Source | Uppsala University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Insomnia is a commonly reported comorbidity for adolescents with psychiatric conditions. It is well-known that insomnia can exacerbate the concurrent psychiatric symptom load. Results from a pilot study shows that outpatients of Children and Youth Psychiatry can improve their sleep and depressive symptoms by receiving internet-based cognitive behavioral therapy for insomnia (iCBT). This study is designed to evaluate implementation of the treatment in routine care.The study will evaluate aspects of the implementation process such as organizational attitudes towards iCBT before implementation, level of knowledge about the condition and intervention among health-care providers before and after the implementation, and clinical outcomes in routine care.
Status | Completed |
Enrollment | 15 |
Est. completion date | October 31, 2020 |
Est. primary completion date | October 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 13 Years to 17 Years |
Eligibility | Inclusion Criteria: - To fulfill the diagnostic criteria for insomnia - To have access to a computer with Internet connection - No previous or ongoing CBT for insomnia Exclusion Criteria: - Ongoing manic or psychotic episode - Being at high risk of triggering manic or psychotic episode - Ongoing sleep apnea |
Country | Name | City | State |
---|---|---|---|
Sweden | Uppsala University Hospital | Uppsala | Uppsala Län |
Lead Sponsor | Collaborator |
---|---|
Uppsala University Hospital | Karolinska University, Uppsala University |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Insomnia Severity Index (ISI; Morin, 1993) | Change in severity of insomnia is assessed by measuring ISI at several measurement points before, during and after treatment. The score ranges from 0-28, higher values indicate worse symptoms of insomnia. | Pre-treatment, weekly for seven weeks (during treatment), after 7 weeks (i.e. post-treatment), after 7 weeks and 4 months (i.e. 4 months after treatment is completed) | |
Secondary | Montgomery-Åsberg Depression Rating Scale - Self report (MADRS-S; Svanborg & Åsberg, 1994) | Change in depressive symptoms is assessed by measuring MADRS-S at several measurement points before, during and after treatment. The score ranges from 0-35, higher values indicate worse symptoms of depression. | Pre-treatment, after 7 weeks (i.e. post-treatment), after 7 weeks and 4 months (i.e. 4 months after treatment is completed) | |
Secondary | Childrens Global Assessment Scale (C-GAS; Shaffer et al., 1983) | Change in clinician-rated level of functioning is assessed by measuring C-GAS at several measurement points before, during and after treatment. The score ranges from 0-100, higher values indicate better functioning. | Pre-treatment, after 7 weeks (i.e. post-treatment), after 7 weeks and 4 months (i.e. 4 months after treatment is completed) |
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