Insomnia Clinical Trial
— AcuSnoozeOfficial title:
Acupressure for Chronic Insomnia in Adults With Chronic Low Back Pain
Verified date | February 2017 |
Source | University of Michigan |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to examine the effect of 6-weeks of relaxation acupressure
compared to stimulating acupressure or a standard of care on sleep and daytime functioning.
Also, to evaluate the ability of teaching acupressure using web-based applications.
It is believed that self-administered relaxation acupressure will result in improvements of
sleep quality and quantity as compared to stimulating acupressure or a standard of care.
Status | Terminated |
Enrollment | 5 |
Est. completion date | December 15, 2013 |
Est. primary completion date | December 15, 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - 18-65 years of age - Meet DSM-IV criteria for primary insomnia - Insomnia must also be documented on two weeks of a baseline sleep diary Exclusion Criteria: - Diagnosis or high clinical suspicion of a sleep disorder other than insomnia - Evidence of a unstable Axis I psychiatric disorder - Evidence of an uncontrolled medical disorder or pain syndrome that affects sleep, causes daytime sleepiness, or is likely to be causally associated with the insomnia - Current pharmacological or non-pharmacological insomnia treatment - Routine overnight shift work - Previous failed trial of acupuncture or acupressure |
Country | Name | City | State |
---|---|---|---|
United States | Domino's Farm | Ann Arbor | Michigan |
Lead Sponsor | Collaborator |
---|---|
University of Michigan |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Difference in the effect of 6-weeks of Relaxation Acupressure compared to Stimulating Acupressure or standard of care on chronic insomnia and daytime functioning. | Insomnia will be assessed/determined by daily sleep/wake diaries and the Insomnia Severity Index questionnaire. Sleep Diary: insomnia = <85% sleep efficiency ratio. Daytime functioning will be determined by the Fatigue Severity Scale of Sleep Disorders (FSS). |
6 weeks | |
Secondary | Success of teaching the acupressure interventions using a novel web-based application measured by an Acupressure Fidelity Form at week 1 and week 6. | The success of learning acupressure via a web-based application will be assessed using an Acupressure Fidelity Form. The form will assess the participants ability to locate each acupressure point, demonstrate proper pressure/technique, and know the frequency of their treatments. Acupressure Form A is worth a total of 12 points while Form B is worth 13 points. Each correct answer is worth 1 point. We will consider our web based intervention "successful" if 95% of participants (49 of them) received a score of 100% at both visits. | 6 weeks |
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