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Treatment of Insomnia in Primary Care Study

Treatment of Insomnia in Primary Care Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06149273
Acronym
TIP
Enrollment
250
Registered
2023-11-28
Start date
2023-12-02
Completion date
2029-12-01
Last updated
2026-05-01

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

Conditions

Insomnia Chronic

Keywords

Cognitive behavioral therapy for insomnia, CBT-I, Primary care, Insomnia severity index, Quality of life, Depressive symptoms

Brief summary

The goal of this clinical trial is to learn about insomnia treatment among primary care patients with chronic insomnia. The main question it aims to answer is: • Does Sleep School (a therapy for insomnia) work well to decrease harm of insomnia? Participants will attend a group therapy intervention once a week for six weeks. Researchers will compare Sleep School to treatment as usual (short counselling by an educated nurse) to see if the Sleep School works better than treatment as usual in decreasing the harm of insomnia.

Interventions

BEHAVIORALSleep School

Sleep school is a structured method for the treatment of insomnia, which is based on cognitive behavioral therapy for insomnia (CBT-I). The central element of the method is a workbook for the patients. The essential parts of the method are strengthening the patient's self-efficacy, introducing the therapeutic exercises, and supporting the continued use of the exercises. The main themes of the Sleep school are information about sleep and the factors affecting it, behavioural components of CBT-I, like restricting the time spent in bed, cognitive components of CBT-I, like constructive worrying -exercise, and the exercises that aim to calm down mind and the autonomic nervous system. The Sleep School is held by an educated nurse.

BEHAVIORALTreatment as usual

Oral and written information about improving sleep habits given by an educated nurse.

Sponsors

University of Turku
Lead SponsorOTHER
University of Eastern Finland
CollaboratorOTHER

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

* Insomnia severity index (ISI) score at least 8 * insomnia symptoms present at least for 3 months

Exclusion criteria

* diagnosed dementia based on medical records * acute suicidality * acute psychotic symptoms

Design outcomes

Primary

MeasureTime frameDescription
Mean Change from Baseline in Insomnia Severity Index (ISI) score at 8 weeksBaseline and Week 8The ISI is a validated self-report tool for assessing the severity, and impact of current insomnia symptoms. It consists of 7 Likert-scale questions with a total score ranging from 0 to 28 (with higher scores indicating more severe insomnia). Change = Week 8 score - Baseline score.

Secondary

MeasureTime frameDescription
Mean change from Baseline in Patient Health Questionnaire 9 (PHQ-9) at 8 weeksBaseline and Week 8PHQ-9 is a validated self-administered instrument assessing each of the 9 Diagnostic and Statistical Manual of Mental Disorders (DSM)-IV criteria for depression as 0 (not at all) to 3 (nearly every day), and the severity of depression. Possible scores range from 0 to 27. Change = Week 8 score - Baseline score.
Mean change from Baseline in EUROHIS Quality of Life 8-item Index at 8 weeksBaseline and Week 8EUROHIS Quality of Life 8-item Index is a validated instrument for the assessment of general quality of life. There are altogether eight questions about the general, physical, psychological, social, and environmental aspects of quality of life. Every question is scored from 1 (very poor) to 5 (very good). All scores can be added together and divided by 8 (the sum of the questions) to obtain the EUROHIS-QOL mean score. Change = Week 8 score - Baseline score.
Mean change from Baseline in Work Ability Score (WAS) at 8 weeksBaseline and Week 8The WAS is the first item of the Work Ability Index (WAI), a validated instrument for the assessment of work ability. WAS is a single question "What is your current work ability compared to your lifetime best?" It has a 0-10 response scale, where 0 stands for "completely unable to work" and 10 stands for "work ability at its best." The WAS has been shown to have a strong association with the WAI and is reliable in evaluating work ability. Change = Week 8 score - Baseline score.

Countries

Finland

Contacts

CONTACTElina Bergman, PhD
elkaro@utu.fi0
CONTACTAnsa Rantanen, PhD
atsipp@utu.fi
PRINCIPAL_INVESTIGATORPäivi Korhonen, PhD

University of Turku

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 2, 2026