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Hip-spine Intervention for Older Adults With Chronic Low Back Pain

University of Delaware logo

University of Delaware

Status

Completed

Conditions

Low Back Pain

Treatments

Behavioral: SFEX
Behavioral: SFEX+H

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Low back pain (LBP) is extremely common in older adults and is associated with a host of negative consequences, including decreased physical function and increased healthcare utilization. Among older adults with LBP, hip impairments indicative of hip joint disease are more prevalent and associated with greater disability than among older adults without LBP. This study will investigate a novel intervention designed to improve LBP-related disability by combining a typical spine-focused exercise program with a hip-focused intervention.

Enrollment

24 patients

Sex

All

Ages

60 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 60-85
  2. Low Back Pain for ≥ 3 months with pain of at least moderate intensity every day or almost every day that requires activity modification.
  3. Presence of at least 1 hip impairment denoted by the American College of Rheumatology as potential indicators of hip osteoarthritis: hip pain, pain on hip internal rotation or morning stiffness of the hip of <60 minutes.

Exclusion criteria

  1. Previous hip fracture repair or total hip replacement
  2. Prominent component of radicular pain: CLBP with distal radiation below the knee
  3. Known spinal pathology other than osteoarthritis: (e.g., a history of back surgery or recent trauma, spinal stenosis, vertebral compression fractures, ankylosing spondylitis, carcinoma metastatic to the spine)
  4. Non-ambulatory, or severely impaired mobility (i.e., require the use of a wheelchair)
  5. Folstein Mini-Mental State Examination score of <24
  6. Severe visual or hearing impairment.
  7. Red flags indicative of a serious disorder underlying the LBP: Red flags that would require specialized medical attention include fever, significant unintentional weight loss, a sudden recent change in the character or intensity of pain, trauma that preceded the onset of pain, or signs and symptoms of caudae equinae (i.e. loss of sensation over saddle region, significant disturbances in bowel and bladder function).
  8. Significant pain in parts of the body other than the back or acute LBP.
  9. Acute, ongoing illness.
  10. Inability to participate in the study for the full six months for any known reason.(i.e. moving away, extended vacation)
  11. Received physical therapy for their LBP within in the last 3 months.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

24 participants in 2 patient groups

SFEX+H
Experimental group
Description:
Participants will receive an intervention consisting of heat to the low back, manual therapy to the hip (including movement of the hip by the therapist), hip-focused strengthening exercises and a trunk muscle training program including exercises for the abdominal and low back muscles.
Treatment:
Behavioral: SFEX+H
SFEX
Active Comparator group
Description:
Participants will receive an intervention consisting of heat to the low back, manual therapy to the hip (including movement of the hip by the therapist) and a trunk muscle training program including exercises for the abdominal and low back muscles.
Treatment:
Behavioral: SFEX

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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