Comparing the Effects of Yoga Nidra to Yoga Nidra With Pain Acceptance Intention and Motor Imagery on Pain Outcomes

Part of paid clinical trials in Orlando, Florida.

Sponsor
University of Central Florida
Study ID
NCT06590181
Status
Recruiting
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Conditions

  • Chronic Pain

Eligibility Criteria

Sex
ALL
Age
18 Years - 75 Years
Healthy Volunteers
Not accepted

Interventions

  • Yoga Nidra — OTHER
    This protocol is derived from The Origin and Clinical Relevance of Yoga Nidra (Pandi-Perumal, S. R. 2022)
  • Yoga Nidra with Pain Acceptance Intention — OTHER
    Yoga Nidra with Pain Acceptance Intention
  • Yoga Nidra with Pain Acceptance Intervention and Motor Imagery — OTHER
    Yoga Nidra with Pain Acceptance Intervention and Motor Imagery

Study Details

Yoga Nidra is a scripted mind-body intervention (MBI) that uses guided relaxation technique in a reproducible sequence of mechanisms that naturally produce a parasympathetic response. This is a randomized controlled trial in which participants will be randomly assigned to one of three interventions: 1) yoga nidra (Yoga Nidra Script Basic), 2) yoga nidra with pain acceptance (Yoga Nidra Acceptance Intention), 3) yoga nidra with pain acceptance and Explicit Motor Imagery (Yoga Nidra Acceptance Intention and Visualization).

Key Dates

Start date
Sep 12, 2024
Status verified
Dec 2024
Primary completion
Sep 15, 2025
Completion
Sep 15, 2025

Study Design

Enrollment
60 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Yoga Nidra
    This protocol is derived from The Origin and Clinical Relevance of Yoga Nidra (Pandi-Perumal, S. R. 2022) and is approximately 20 minutes total time.
  • Active Comparator: Yoga Nidra and Pain Acceptance Intention
    Yoga Nidra plus a Pain Acceptance Intention.
  • Active Comparator: Yoga Nidra with Pain Acceptance Intervention and Motor Imagery
    Yoga Nidra plus pain acceptance and motor imagery

Primary Outcome Measure

Pressure Pain Threshold [ Time Frame: Pre/Post intervention, Day 1 ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of Central FloridaOrlandoFlorida32816
[email protected]
407-823-1026

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By research site
University of Central Florida· Orlando, FL

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