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OpenTrials
Completed

NCT Number: NCT04571593

Remote Yoga Nidra for Anxiety and Sleep

The goal of this application is to collect survey data indicating the effects of a digital Yoga Nidra practice on anxiety and sleep during COVID-19. We will explore effects on momentary anxiousness, as well as on sleep. Participants will be consented through REDCap during the Yoga Nidra class, then asked to complete an intake form, a sleep questionnaire (composed of questions from the Post Sleep Questionnaire (PSQ)) and a pre/post State Trait Anxiety (STAI) Index, surrounding the practice. Participants will receive an email the next morning, inquiring about their sleep (~2 min survey), and again the following week, the morning of the Yoga Nidra class, in order to remind them about the weekly class offering and also to collect sleep data for a night that did not include pre-bed Yoga Nidra. We will additionally report feasibility measures including enrollment, retention, qualitative feedback, and challenges of using the digital platform. Using this data, we will gain valuable feasibility data for implementation of this type of mind-body practice using digital platforms. We will also gain important data on the effects of this practice on anxiety and sleep.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National University of Natural Medicine, Helfgott Research Institute

Portland, Oregon, 97201, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults
  • Can understand a recording in English while resting comfortably

Exclusion criteria

NA

Treatment and study plan

Yoga Nidra

Behavioral

The practice of Yoga Nidra, is a scripted and reproducible, guided meditation technique that promotes mental, emotional and physical relaxation while also facilitating the transition between waking and sleeping.

Primary outcomes

  1. Change in Momentary Anxiety

    Time frame: Pre-intervention and immediately after the intervention

    State Trait Anxiety (STAI-6) Short Form (scale 20 to 80, with higher scores indicating higher momentary anxiety)

  2. Change in Sleep Quality

    Time frame: Baseline (pre-intervention), 1 day (morning after intervention), and 2-6 days later (survey sent each Tuesday, to capture a night without Yoga Nidra)

    Post Sleep Questionnaire (PSQ): six questions

Secondary outcomes

  1. Incidence of Intervention-Emergent Challenges as assessed by a Feedback Survey

    Time frame: Post-intervention (survey sent at 16 weeks)

    Qualitative Feedback Survey (developed in-house)

  2. Satisfaction as assessed by a Feedback Survey

    Time frame: Post-intervention (survey sent at 16-weeks)

    Qualitative Feedback Survey (developed in-house)

Sponsors and collaborators

Lead sponsor

National University of Natural Medicine

Other

Registry information

Official study title

Digital Delivery of Yoga Nidra for Anxiety and Sleep: A Feasibility Study

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Oct 1, 2020
Registry last updated
Nov 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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