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Clinical Trials/KCT0002685
KCT0002685
Recruiting
未知

A study of evaluating the reliability and validity of Pattern Identifications Tool for Insomnia(PIT-I) and analyzing correlation with psychological tests

Dunsan Korean Medicine Hospital of Daejeon University0 sites38 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Dunsan Korean Medicine Hospital of Daejeon University
Enrollment
38
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Observational Study
Sex
All

Investigators

Sponsor
Dunsan Korean Medicine Hospital of Daejeon University

Eligibility Criteria

Inclusion Criteria

  • 1\) Male and female subjects aged 19 to 64
  • 2\) Those with an Insomnia Severity Index (ISI) score of 15 or higher
  • 3\) Those who meet DSM\-V sleep disorder diagnosis criteria
  • 4\) After hearing the purpose and characteristics of this clinical study, he / she voluntarily agrees to participate and signs the consent form

Exclusion Criteria

  • 1\) Those who have been treated for sleeplessness or for medicinal or herbal medicines within the last 2 weeks as needed for improvement of sleeplessness, or regularly taking medication has changed in type or dosage within the last 4 weeks
  • 2\) Those diagnosed with major mental disorders such as major depressive disorder, anxiety disorder, panic disorder, or diagnosed with addiction to caffeine, alcohol, or drugs
  • 3\) Shift work which can clearly affect life cycle, person who changes working hours of the night
  • 4\) Those who have clear pain that may interfere with sleeping or a disease that may cause sleeping
  • 5\) Those who are suspected of having uncontrolled hormonal disease, severe disease, systemic disease (eg, hyperthyroidism, chronic liver disease, chronic renal disease)
  • 6\) If it is deemed difficult to comply with treatment, visit, questionnaire, etc.
  • 7\) If the clinical researcher judges that it is inappropriate
  • 8\) Those who have participated in other clinical trials in a month before this study or are planning to participate in other clinical trials during the trial period

Outcomes

Primary Outcomes

Not specified

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