Lumbosacral Spinal Stenosis - Non-Invasive Postural Therapy for Older Adult Veterans

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age55-80
SponsorVA Office of Research and Development

About this trial

Lumbosacral spinal stenosis (LSS) is a leading cause of limited mobility, reduced independence, and poor health outcomes in older adults, and is very common in older adult Veterans. Several years ago, major research studies indicated that surgery for LSS was more effective than usual (medical) management. Nonetheless, there are many patients for whom surgery is not the ideal therapy. There have been reports that modifications in daily activities including temporary use of a modified rolling walker and changes in sleep positioning may help relieve LSS. The investigators have assembled a VA team to study this carefully. The investigators will recruit a small group of older adult Veterans with LSS to try out this program; the investigators will monitor them closely for relief of their symptoms and improvements in walking. The investigators will, as part of this small study, try to understand potential barriers to use of this therapy. The investigators will interview the Veterans and healthcare providers to identify problems that may arise in trying this therapy. If this small study works, the investigators plan to expand the effort.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Veterans receiving care at participating VA

Ability to read and write English and understand instructions

Agrees to comply with instructions

Symptoms for over 3 months

Disqualifiers

Previous Low Back Surgery for SS including decompression or fusion

Successful Spinal Stenosis Treatment (such as injection) over the prior 3 months

X ray, CT, or MRI shows Lumbar Spinal Stenosis in 3 or 4 levels

Prior Lumbar Fracture

Trial design

Design model

Single group

Treatments tested in this trial

  • NIPT

    Other intervention

    Coordinated suite of DME and training to support continuous maintenance of flexion posture during the 6 week trial.

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: FeasibilityExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in mobility by actigraph (positive, negative, or zero) as determined by the difference in mobility at Week 6 compared to baseline

Actigraph mobility

Time frame
Week 6

Secondary outcomes

Other outcomes

Sponsors and contacts

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