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Evaluation of Yoga for Sleep Disturbances in Post Traumatic Stress Disorder (PTSD)

Mass General Brigham logo

Mass General Brigham

Status

Completed

Conditions

Post Traumatic Stress Disorder
Insomnia

Treatments

Behavioral: Yoga treatment

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01556074
18180 (Other Grant/Funding Number)
2012P000263
F32AT006092-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The primary objective of this preliminary study is to estimate sleep outcome effect sizes and determine feasibility for a novel yoga treatment of insomnia in participants with post traumatic stress disorder (PTSD). Additional objectives are to evaluate relationships of sleep outcomes with measures of other PTSD symptoms, psychosocial health and possible mechanisms of action.

Enrollment

50 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male and non-pregnant female adults at least 18 years of age.
  • A DSM-IV-TR diagnosis of post-traumatic stress disorder (PTSD).
  • Naïve to yoga and other meditative practices, defined as less than one hour per week for the past 6 months.
  • Potential subjects receiving ongoing medical or psychological treatment are eligible, as long as treatment remains stable over the course of the study and does not include more than one hour weekly of mind-body medicine (strategies directly related to meditation and yoga).
  • No more than 2 alcoholic or caffeinated drinks/day
  • No illicit drug use
  • Potential subjects are eligible if they have been on stable dosage (not PRN) of medication for PTSD symptoms including sleep disturbances and any medication that may influence sleep for at least 6 weeks prior to the study, and be willing to continue with same dosage for the duration of the study.
  • No current substance abuse, defined as diagnosis of substance abuse or dependence disorder within the past year, and/or in/outpatient treatment for substance abuse or dependence in the past 6 weeks.
  • No transcontinental travel over the course of the study.
  • No night-shift or rotating shift work over the course of the study.
  • Insomnia based on the American Academy of Sleep Medicine's Research Diagnostic Criteria (RDC) for insomnia due to a mental health disorder
  • Potential subjects are eligible to participate in this study if they have sufficient mental and physical ability to fully participate in the parameters of the study. Subjects must be able to understand and comply with instructions in the group yoga sessions and home practice, complete questionnaires, participate in clinical interviews, and take part in all data collection activities. Subjects with severe mental or physical concerns that may prevent them from understanding and/or complying with the treatment will be excluded. For example, potential subjects confined to wheelchairs will not be eligible, although subjects with artificial limbs who are able to reasonably participate in the intervention may be deemed eligible. These determinations will be made during discussions with potential subjects on a case by case basis during the screening process.

Exclusion criteria

  • Potential subjects are ineligible if pregnant.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

Yoga treatment
Experimental group
Treatment:
Behavioral: Yoga treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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