Comparing Yoga Nidra, Yoga, and Control Condition on Pain in Individuals With Chronic Low Back Pain

ConditionLow Back Pain
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorUniversity of Central Florida

About this trial

Individuals with chronic low back pain will undergo a yoga, yoga nidra, and control condition on separate visits. Each visit, before and after the intervention, participants with rate their pain in response to heat stimuli, a sit to stand task, and questionnaires.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

low back pain classified as symptoms localized to the posterior region of the trunk, extending from the lower margin of the last rib to the gluteal folds

low back pain for three months or longer with a average pain intensity = 3/10 on the 11-point numeric pain rating scale (NPRS) within the previous twenty-four hours

experienced three or more low back pain episodes within the past 3 years

fluency in English

Disqualifiers

systemic or neurological conditions that could alter sensation (e.g., uncontrolled diabetes)

any surgery or fracture within 6 months

blood-clotting disorders or contraindications to pressure and heat stimuli

current pregnancy and requirement for medical clearance to exercise (screened with Physical Activity Readiness Questionnaire-Plus PAR-Q+

Trial design

Design model

Single group

Treatments tested in this trial

  • Yoga

    Other intervention

    Participants will complete a series of yoga poses.

  • Yoga Nidra

    Other intervention

    Participants will complete yoga nidra, a guided meditation.

  • Control Condition

    Other intervention

    Participants will listen to a story.

Treatment groups

27 Participants
are divided into 3 treatment groups
Group A: YogaExperimental treatment 1 intervention
Group B: Yoga NidraActive comparator 1 intervention
Group C: Neutral ControlPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Heat Pain Threshold

Participants will undergo heat pain threshold. A thermode will be applied to the low back with temperature increasing at 1 degree Celsius per second. Participants will report when the sensation changes from heat to pain and the temperature recorded.

Time frame
through study completion, typically 2 weeks
2

Temporal Summation

Participants will apply thermode to the bottom of the foot and rate their pain in response to 10 heat pulses peaking at 49 degrees Celsius.

Time frame
through study completion, typically 2 weeks

Secondary outcomes

1

Pain Catastrophizing Scale

Participants will complete the pain catastrophizing scale.

Time frame
through study completion, typically 2 weeks
2

Five Times Sit to Stand

Participants with stand up and sit down from a chair five times. The time to complete this task will be recorded.

Time frame
through study completion, typically 2 weeks

Other outcomes

Sponsors and contacts

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