Skip to main content
Clinical Trials/NCT06730178
NCT06730178
Completed
Not Applicable

Calo Psychiatric Center

Calo Psychiatric Center0 sites24 target enrollmentJanuary 1, 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sleep Disorder; Insomnia Type
Sponsor
Calo Psychiatric Center
Enrollment
24
Primary Endpoint
the improvement of relaxation training tape
Status
Completed
Last Updated
last year

Overview

Brief Summary

Background: The purpose of this study was to examine the improvement in insomnia patients using Relaxation Training, and to use the Generalized Estimating Equation model (GEE-I) to analyze the results of repeated measurements and observe the difference between the subjective perception and the objective measurement of sleep duration.

Methods: There were 24 subjects diagnosed as insomnia who completed the treatment course and 5 times evaluation. Of the 24 subjects, 7 accepted the sleep electroencephalogram (EEG). Relaxation training shortened the duration of sleep onset time and decreased the frequency of night awakening.

Detailed Description

Of 47 qualified subjects, 24 volunteers took part in this study after the researchers had explained the study process.The patients were asked to keep a sleep diary. In the diaries, they recorded the time they went to bed and fell asleep, the duration to sleep onset (from "go to the bed" to "fall asleep"), the frequency of night waking, the time of getting up, and any medication history. Patients were instructed to perform the treatment in the evening, preferably just before bedtime, total time was 15 minutes.The patients recorded their sleep conditions every day and underwent relaxation training intervention for 4 weeks.

Registry
clinicaltrials.gov
Start Date
January 1, 2009
End Date
October 30, 2009
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Calo Psychiatric Center
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • All subjects had been diagnosed as having primary insomnia or insomnia related to medical and psychiatric comorbid diagnoses using the D Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) diagnostic criteria.

Exclusion Criteria

  • Patients who had comorbid serious medical illnesses, and pregnant and lactating women were excluded.

Outcomes

Primary Outcomes

the improvement of relaxation training tape

Time Frame: 4 weeks

Participants were instructed to perform the treatment in the evening, preferably just before bedtime, total time was 15 minutes.

Similar Trials