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

NCT ID: NCT06590181

Last Updated: 2024-12-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-09-12

Study Completion Date

2025-09-15

Brief Summary

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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).

Detailed Description

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Conditions

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Chronic Pain

Keywords

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chronic pain meditation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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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.

Group Type EXPERIMENTAL

Yoga Nidra

Intervention Type OTHER

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

Yoga Nidra and Pain Acceptance Intention

Yoga Nidra plus a Pain Acceptance Intention.

Group Type ACTIVE_COMPARATOR

Yoga Nidra with Pain Acceptance Intention

Intervention Type OTHER

Yoga Nidra with Pain Acceptance Intention

Yoga Nidra with Pain Acceptance Intervention and Motor Imagery

Yoga Nidra plus pain acceptance and motor imagery

Group Type ACTIVE_COMPARATOR

Yoga Nidra with Pain Acceptance Intervention and Motor Imagery

Intervention Type OTHER

Yoga Nidra with Pain Acceptance Intervention and Motor Imagery

Interventions

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Yoga Nidra

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

Intervention Type OTHER

Yoga Nidra with Pain Acceptance Intention

Yoga Nidra with Pain Acceptance Intention

Intervention Type OTHER

Yoga Nidra with Pain Acceptance Intervention and Motor Imagery

Yoga Nidra with Pain Acceptance Intervention and Motor Imagery

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Central Florida

OTHER

Sponsor Role lead

Responsible Party

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Abigail Wilson

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Abigail Anderson, PT, DPT, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Central Florida

Locations

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University of Central Florida

Orlando, Florida, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Abigail Anderson, PT, DPT, PhD

Role: CONTACT

Phone: 407-823-1026

Email: [email protected]

Facility Contacts

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Role: primary

Other Identifiers

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YN10

Identifier Type: -

Identifier Source: org_study_id