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Yoga vs Stretching in Veterans With Chronic Lower Back Pain: Does Mindfulness Matter?

Yoga vs Stretching in Veterans With Chronic Lower Back Pain: Does Mindfulness Matter?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03432169
Enrollment
20
Registered
2018-02-14
Start date
2018-02-01
Completion date
2018-12-31
Last updated
2019-10-10

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

Conditions

Chronic Low Back Pain

Brief summary

The purpose of this study is to demonstrate the feasibility of recruiting, enrolling and collecting outcome data on CLBP patients within the Veterans Affairs Community Based Rochester Outpatient Center who undergo an 8 week active exercise class with mindfulness (yoga) and without mindfulness (stretching class)

Detailed description

The study will approach all new or existing patients within the chiropractic clinic between the ages of 18 and 89 who have low back pain greater than 12 weeks and pain greater than or equal to 3, who have no contraindications to active exercise. Patients will be queried as to interest and those interested will be consented. The investigators will recruit a total of 20 patients. Patients will then be randomized to receive either an 8 week active exercise class with mindfulness (yoga) or an 8 week active exercise class without mindfulness (stretching class). Both groups will have home exercise requirements and will be held accountable through the use of a home practice log. Outcomes will include: Pain (PEG), Quality of Life (PROMIS Global Health Survey GHS), Self Efficacy (2 Question), Fear Avoidance Belief, Castrophizing and Social Engagement. Outcomes will be collected at baseline, and again at the end of the 8 week intervention. Clinician open ended questionnaire will be given to both study clinicians at the end of the trial.

Interventions

OTHERYoga (stretching plus mindfulness)

Stretching plus mindfulness

OTHERStretching

Stretching alone

Sponsors

Canandaigua VA Medical Center
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Masking description

Will code data entered into database.

Intervention model description

Group A receives Yoga (stretching with mindfulness) and Group B receives stretching (stretching without mindfulness)

Eligibility

Sex/Gender
ALL
Age
18 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* Adult Veterans between the ages of 18-89 * Lower back pain \> 12 weeks * Have the ability to exercise independently.

Exclusion criteria

* Subjects will be excluded if * They are currently enrolled in or maintain a home meditation practice * If they are currently involved in a mindfulness or cognitive behavioral therapy group. * If they have participated in a structured group yoga class in the last three months. * If they have an open workers compensation or no-fault case or have undergone spinal surgery in the past 6 months.

Design outcomes

Primary

MeasureTime frameDescription
Feasibility6 monthsThe main purpose of the study is to assess feasibility of conducting a larger trial. The study team will assess number of Veterans recruited and enrolled in the study. Number of sessions completed.

Secondary

MeasureTime frameDescription
PROMIS Global Health Scale (GHS):baseline, immediately post interventionPatient reported outcome measurement information system has developed a quality of life tool that provides an overall index score for quality of life. This form has recently been validated in comparison to the EuroQual. T-Score distributions are standardized such that a 50 represents the average (mean) for the US general population, and the standard deviation around that mean is 10 points. A high score always represents more of the concept being measured.
Pain, Engagement and General activity (PEG)baseline, immediately post interventionAn ultra-brief three-item scale derived from the Brief Pain Inventory (BPI), was a reliable and valid measure of pain among primary care patients with chronic musculoskeletal pain and diverse VA ambulatory patients.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026