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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06590181
Enrollment
60
Registered
2024-09-19
Start date
2024-09-12
Completion date
2025-07-29
Last updated
2026-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain

Keywords

chronic pain, meditation

Brief summary

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).

Interventions

This protocol is derived from The Origin and Clinical Relevance of Yoga Nidra (Pandi-Perumal, S. R. 2022)

OTHERYoga Nidra with Pain Acceptance Intention

Yoga Nidra with Pain Acceptance Intention

OTHERYoga Nidra with Pain Acceptance Intervention and Motor Imagery

Yoga Nidra with Pain Acceptance Intervention and Motor Imagery

Sponsors

University of Central Florida
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Chronic pain in the neck, low back, shoulder, hip, elbow, knee, wrist, or ankle that has lasted for over three months * Pain intensity rated as 3/10 or higher in the past 24 hours (0=no pain, 10=worst pain imaginable)

Exclusion criteria

* non-English speaking * systemic medical conditions that affect sensation (such as uncontrolled diabetes) * History of surgery or fracture within the past six months * any blood clotting disorders (such as hemophilia) * any contraindication to the application of ice (blood pressure \> 140/90 mmHg, cold urticaria, cryoglobulinemia, paroxysmal cold hemoglobinuria, circulatory compromise) * Exceed pressure and heat sensory thresholds * Unable to access internet or email * Pregnant

Design outcomes

Primary

MeasureTime frameDescription
Pressure Pain ThresholdPre/Post intervention, Day 1A computerized pressure algometer (AlgoMed, Ramat Yishai, Israel) with a 1 cm diameter rubber tip will be applied to the upper trapezius.
Temporal SummationPre/Post intervention, Day 1Change in pain ratings during 10 heat pulses will be recorded.
Conditioned Pain ModulationPre/Post intervention, Day 1Pressure pain threshold after a cold water immersion task.
Heat Pain ThresholdPre/Post intervention, Day 1Participants will report when comfortable heat becomes painful by pressing a button. Temperature in degrees Celsius will be recorded at threshold

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAbigail Anderson, PT, DPT, PhD

University of Central Florida

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 27, 2026