Hip-spine Intervention for Older Adults With Chronic Low Back Pain
Pilot Trial of a Hip-spine Intervention for Older Adults With a Primary Complaint of Low Back Pain
1 other identifier
interventional
24
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable low-back-pain
Started Feb 2017
Typical duration for not_applicable low-back-pain
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 23, 2017
CompletedFirst Posted
Study publicly available on registry
January 25, 2017
CompletedStudy Start
First participant enrolled
February 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 13, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
March 13, 2018
CompletedOctober 9, 2018
October 1, 2018
1.1 years
January 23, 2017
October 8, 2018
Conditions
Outcome Measures
Primary Outcomes (2)
Quebec Low Back Pain Disability Scale
Change in disability score from pre-intervention to 20 weeks later
Patient-Specific Functional Scale
Change in pain-related function score from pre-intervention to 20 weeks later
Secondary Outcomes (2)
Walking Endurance as measured by the 6 minute walk test
Change in walking endurance from pre-intervention to 20 weeks later
Walking speed
Change in walking endurance from pre-intervention to 20 weeks later
Study Arms (2)
SFEX+H
EXPERIMENTALParticipants 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.
SFEX
ACTIVE COMPARATORParticipants 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.
Interventions
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. The intervention will be delivered twice weekly for 8 weeks.
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. The intervention will be delivered twice weekly for 8 weeks.
Eligibility Criteria
You may qualify if:
- Age 60-85
- Low Back Pain for ≥ 3 months with pain of at least moderate intensity every day or almost every day that requires activity modification.
- 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.
You may not qualify if:
- Previous hip fracture repair or total hip replacement
- Prominent component of radicular pain: CLBP with distal radiation below the knee
- 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)
- Non-ambulatory, or severely impaired mobility (i.e., require the use of a wheelchair)
- Folstein Mini-Mental State Examination score of \<24
- Severe visual or hearing impairment.
- 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).
- Significant pain in parts of the body other than the back or acute LBP.
- Acute, ongoing illness.
- Inability to participate in the study for the full six months for any known reason.(i.e. moving away, extended vacation)
- Received physical therapy for their LBP within in the last 3 months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Delaware
Newark, Delaware, 19713, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
January 23, 2017
First Posted
January 25, 2017
Study Start
February 1, 2017
Primary Completion
March 13, 2018
Study Completion
March 13, 2018
Last Updated
October 9, 2018
Record last verified: 2018-10
Data Sharing
- IPD Sharing
- Will not share