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Low Back PainNCT07543835

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

A study testing Yoga and Yoga Nidra in people with Low Back Pain, run by University of Central Florida at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Low Back Pain
What is being tested?
Yoga and Yoga Nidra
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
27 participants
Where
1 siteUnited States
Study dates
25 Aug 2026to 1 Jul 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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
  • ability to attend all visits
  • reliable email access.

Who cannot join

  • 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+
  • not receiving physical therapy or chiropractor treatments for low back pain

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Abigail Anderson Assistant Professor contact

407-823-1026

Abigail.Wilson@ucf.edu

United States1 site, 1 recruiting
  • University of Central Florida

    Orlando, Florida, 32816

    Abigail Anderson Assistant Professor, 407-823-1026, Abigail.Wilson@ucf.edu

    Recruiting

Other trials in United States

About this study

Official title: Comparing the Effects of Yoga Nidra, Yoga, and Control Condition on Thermal Pain Processing, Psychological Factors, and Movement-Evoked Pain in Individuals With Chronic Low Back Pain

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.

Conditions
Low Back Pain
Being tested
Yoga, Yoga Nidra, Control Condition
Keywords
low back pain, yoga
Medical subject headings
Low Back Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • YogaOther

    Participants will complete a series of yoga poses.

  • Yoga NidraOther

    Participants will complete yoga nidra, a guided meditation.

  • Control ConditionOther

    Participants will listen to a story.

Study groups in NCT07543835
Study groupRoleWhat they receive
YogaExperimentalParticipants will complete a series of guided yoga poses.
Receives: Other: Yoga
Yoga NidraActive comparatorParticipants will complete yoga nidra, a guided meditation.
Receives: Other: Yoga Nidra
Neutral ControlPlacebo comparatorParticipants will listen to a story.
Receives: Other: Control Condition

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: 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.

    Measured: through study completion, typically 2 weeks

Secondary outcomes (2)
  1. Pain Catastrophizing Scale

    Participants will complete the pain catastrophizing scale.

    Measured: 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.

    Measured: through study completion, typically 2 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Apr 2026
  2. Study start25 Aug 2026
  3. Primary completion1 Jul 2027 (estimated)
  4. Study completion1 Jul 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Single group
Masking
None (open label)
Enrolment
27 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07543835
Sponsor's protocol ID
13
Status last verified
Aug 2026
First submitted
8 Apr 2026
Last updated
2 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Yoga and Yoga Nidra in people with Low Back Pain, run by University of Central Florida at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 2 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Abigail Anderson Assistant Professor (407-823-1026, Abigail.Wilson@ucf.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Heat Pain Threshold (time frame: through study completion, typically 2 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Sep 2026.

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