Status:

RECRUITING

Yoga Nidra for Insomnia and Posttraumatic Stress Symptoms

Lead Sponsor:

University College, London

Collaborating Sponsors:

National Institute of Mental Health (NIMH)

Conditions:

Posttraumatic Stress Disorder (PTSD)

Insomnia

Eligibility:

All Genders

18-35 years

Phase:

NA

Brief Summary

This randomized feasibility study is designed to investigate the feasibility of recruitment and delivery of two variations (brief; full) of a virtual Integrative Restoration (iRest) yoga nidra meditat...

Detailed Description

Participants will be randomly assigned to 1 of three groups: two remote yoga nidra interventions will be compared to a waitlist control group. The yoga nidra groups will be as follows: a high-dose con...

Eligibility Criteria

Inclusion

  • Endorses experiencing at least one lifetime very stressful or traumatic event that still distresses them
  • Score of 13 or higher on the 8-item PCL-5
  • Scoring 15 or higher on the Insomnia Severity Index, indicating the presence of moderate to severe insomnia
  • Being able and willing to listen to online yoga nidra audio recordings that may each be up to 35 minutes long daily for 8 weeks
  • Being willing to monitor sleep and PTSD symptoms for 10 weeks
  • Normal or corrected to normal hearing and vision
  • Fluent in English
  • Reliable daily access to the internet Between the ages of 18 and 35
  • Between the ages of 18 and 35
  • Reliable daily access to the internet
  • Willing to refrain from ingesting caffeine, alcohol, and recreational drugs the day of the sleep studies
  • Currently receiving or seeking treatment for alcoholism or a substance abuse disorder

Exclusion

  • History of schizophrenia, psychotic disorder, or bipolar disorder
  • Current endorsement of suicidality (score of 2 or higher on Item 9 of the BDI-II)
  • Currently receiving psychological treatment for any mental health disorder
  • Current diagnosis of any sleep disorder, excluding insomnia or nightmare disorder
  • Currently taking benzodiazepines, nonbenzodiazepine receptor agonists, orexin agonists or antagonists, antiseizure medication, any medications for sleep
  • Score of 5 or higher on STOP-BANG Questionnaire (indicating likelihood of moderate to severe obstructive sleep apnea)
  • Previous adverse experience with meditation
  • Current regular meditative practice (meditating once or more per month)

Key Trial Info

Start Date :

March 3 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

November 1 2025

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT06888336

Start Date

March 3 2025

End Date

November 1 2025

Last Update

March 21 2025

Active Locations (1)

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1

University College London

London, United Kingdom