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Internet-CBT for Insomnia

Guided Internet-treatment for Insomnia. Treatment Effects, Health Economics and Interaction With Depression

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01256099
Acronym
IpsyInsomni
Enrollment
191
Registered
2010-12-08
Start date
2010-01-31
Completion date
2015-02-28
Last updated
2015-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Insomnia

Keywords

Self-help treatment, Internet treatment, CBT, Prevention, Comorbidity

Brief summary

This study includes two sub-trials. In trial 1 patients suffering from insomnia but not meeting the criteria for depression are randomised to either therapist guided Internet-based CBT for insomnia or to a control group with a non-guided, brief self-help program that acts as a placebo control. The primary purpose is to evaluate reduction in Insomnia severity (compared to placebo) after treatment and at follow-ups at 6-month, 1 year and 3 years. Secondary purpose is to evaluate the costeffectiveness of the treatment and to evaluate if the insomnia treatment has a preventive effect on future depressive episodes. Recruitment is done through mass media and includes all regions of Sweden. Initial assessment based on questionnaires and telephone interviews. Trial 2 includes patients suffering from both Insomnia and depression. Randomization is done between either CBT for insomnia or CBT for depression (both Internet-based) to evaluate each respective treatment's effect on both insomnia and depression. The patients need for further treatment after the initial one will be measured and used as a secondary outcome. Recruitment is done through mass media but only citizens in the Stockholm area are included since the initial assessment are based on both questionnaires and telephone interviews as well as a visit at a psychiatrist located at the Internet psychiatry clinic in Stockholm. Both trials will include health economic data and analysis. For the longer follow-up periods (1 and 3 years), registers will be used to analyse consumption of sleep medication and antidepressants as well as general health care utilization.

Interventions

An 8 week long, structured self-help program with weekly reports to, and feedback from, a CBT therapist over the Internet. Includes traditional CBT-methods for insomnia

BEHAVIORALBrief Internet-CBT for insomnia, without support

No support and less text, not including the CBT-methods that are presumed to be most effective to reduce Insomnia symptoms

BEHAVIORALTherapist Guided Internet-CBT for depression

An 9 week long, structured self-help program with weekly reports to, and feedback from, a CBT therapist over the Internet. Includes traditional CBT-methods for depression. Information and methods regarding sleep difficulties removed

Sponsors

Region Stockholm
CollaboratorOTHER_GOV
Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Clinical level of Insomnia (more than 10 on ISI) * Meets criteria for Insomnia according to DSM-IV-TR * Enough language skills * Only Trial 2: Meets criteria for Major Depressive Disorder according to DSM-IV-TR

Exclusion criteria

* Sleep disorders requiring other treatment * High consumption of alcohol/drugs that affect sleep * Started to use or changed the dose of antidepressant drug during the last 2 months * Somatic or psychiatric conditions requiring acute care * Working night shifts * Only Trial 1: Meets criteria for Major Depressive Disorder according to DSM-IV-TR

Design outcomes

Primary

MeasureTime frameDescription
Insomnia Severity Index (ISI)Post-treatment (9 weeks)7-item, self-rated questionnaire measuring insomnia severity. Bastien, C. H., Vallières, A., & Morin, C. M. (2001). Validation of the Insomnia Severity Index as an outcome measure for insomnia research. Sleep Medicine, 2, 297-307.
MADRS-SPost-treatment (9 weeks)The use of two primary outcomes are motivated since the purpose is to look at effects on both insomnia and depression. In trial 1 the former is used to predict the latter, and in Trial 2 the patientents suffer from both conditions. The MADRS-S is a 9-item self-rated measure of depression severity and screens for suicidality. Mattila-Evenden, M., Svanborg, P., Gustavsson, P., & Åsberg, M. (1996). Determinants of self-rating and expert rating concordance in psychiatric out-patients, using the affective subscales of CPRS. Acta Psychiatr Scand, 94, 386-396.
ISI6-month follow-up

Secondary

MeasureTime frameDescription
Sleep DiarySame as primary outcomesOne week of self-ratings on a number of sleep parameters, resluting in measures of sleep latency, total sleep time, sleep efficacy, number of nighttime awakenings, subjecitve sleep quality and daytime functioning
Trimbos and Institute of Medical Technology Assessment Cost Questionnaire for Psychiatry (TIC-P)Same as Primary outcomesHealth economic questionnaire evalutation cost for health care, abscence of work capacity and related costs. Hakkaart-Van Roijen, L.,Van Straten, A., & Donker, M. (2002). Manual: Trimbos/iMTA Questionnaire for Costs Associated with Psychiatric Illness. Rotterdam: Erasmus University
EQ-5DSame as primary outcomesGeneral quality of life measure to complement the TIC-P in health economic analysis. Hinz, A., Klaiberg, A., Brahler, E., & Konig, H.H. (2006). The Quality of Life Questionnaire EQ-5D: modelling and norm values for the general population. Psychother.Psychosom.Med.Psychol., 56, 42-48.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026