Improving Sleep and Quality of Life in Adults With HIV Disease (R&R)

This study has been completed.
Sponsor:
Information provided by:
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT01073423
First received: February 17, 2010
Last updated: June 22, 2010
Last verified: June 2010

February 17, 2010
June 22, 2010
January 2010
April 2010   (final data collection date for primary outcome measure)
self-reported sleep disturbance [ Time Frame: 8 weeks ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01073423 on ClinicalTrials.gov Archive Site
  • actigraphic estimates of sleep quality and quantity [ Time Frame: 8 weeks ] [ Designated as safety issue: No ]
  • self-reported well-being [ Time Frame: 8 weeks ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Improving Sleep and Quality of Life in Adults With HIV Disease
Improving Sleep and Quality of Life in Adults With HIV Disease: A Pilot Study

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

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Insomnia
  • Behavioral: Music Therapy
    1-hour music therapy sessions, administered in group format 3 times per week for 8 weeks.
  • Behavioral: Yoga
    1-hour yoga sessions administered in group format 3 times per week for 8 weeks
  • Experimental: Yoga
    Intervention: Behavioral: Yoga
  • Active Comparator: Music Therapy
    Intervention: Behavioral: Music Therapy
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
20
April 2010
April 2010   (final data collection date for primary outcome measure)

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
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
NCT01073423
R&R Pilot
No
Kathryn A. Lee / Associate Dean of Research, University of California, San Francisco
University of California, San Francisco
Not Provided
Principal Investigator: Kathryn A. Lee, RN, PhD University of California, San Francisco
University of California, San Francisco
June 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP