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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01073423
Other study ID # R&R Pilot
Secondary ID
Status Completed
Phase N/A
First received February 17, 2010
Last updated June 22, 2010
Start date January 2010
Est. completion date April 2010

Study information

Verified date June 2010
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see if yoga or music therapy can improve the sleep of adults with HIV.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date April 2010
Est. primary completion date April 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- at least 18 years of age

- HIV seropositive

- current sleep disturbance

- able to speak, read, and write in English

- a phone number to maintain contact with research team

- willing to provide copy of most recent CD4 and viral load values

- willing to wear actigraph for 1 week per month for 3 months

- willing to participate in group intervention sessions 3 times per week for 8 weeks

Exclusion Criteria:

- pregnancy

- psychiatric diagnosis, such as schizophrenia, dementia, bipolar disorder (depression not excluded)

- sleep disorder diagnosis, such as apnea or narcolepsy (insomnia not excluded)

- current yoga practice

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Music Therapy
1-hour music therapy sessions, administered in group format 3 times per week for 8 weeks.
Yoga
1-hour yoga sessions administered in group format 3 times per week for 8 weeks

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Francisco

Outcome

Type Measure Description Time frame Safety issue
Primary self-reported sleep disturbance 8 weeks No
Secondary actigraphic estimates of sleep quality and quantity 8 weeks No
Secondary self-reported well-being 8 weeks No
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