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Effectiveness of Therapeutic Exercises on Spinopelvic Mobility

Effectiveness of Therapeutic Exercises on Spinopelvic Mobility

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06838455
Enrollment
53
Registered
2025-02-20
Start date
2025-02-28
Completion date
2025-12-31
Last updated
2025-02-20

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

Conditions

Osteoarthritis (OA) of the Hip

Brief summary

The purpose of this study is to examine the extent to which spinopelvic exercises may affect either sagittal spinal deformity or spinopelvic mobility and identifying patients at risk for hip instability following a total hip replacement.

Interventions

OTHERSpinopelvic mobility exercise

Participants will complete a 15-20 min session of therapeutic exercises performed by patients with assistance of a pre-recorded video. The exercise regimen has been developed by the investigators of this study to incorporate exercises to increase a patient's spinopelvic mobility. Study staff that has been properly trained will be present to guide the patient through the exercise regimen and ensure the exercises are being performed accurately.

Sponsors

Colorado Joint Replacement
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

1. Patients aged 18-90 scheduled for total hip arthroplasty 2. Patients with primary hip osteoarthritis 3. Patients with or without history of prior spinal injections

Exclusion criteria

1. Patients undergoing revision total hip arthroplasty. 2. Patients with spinal fusion. 3. Patients who exercised prior to radiographic analysis. 4. Patients unable to complete imaging at the designated time of day. 5. Symptomatic contralateral hip osteoarthritis. 6. Patients unwilling or unable to perform therapeutic exercise program as instructed. This includes patients requiring use of assistive devices or who would be deemed unsafe to perform the exercises without a 1- or 2-person assist.

Design outcomes

Primary

MeasureTime frameDescription
Spinopelvic radiographic measurementsChange from baseline to up to 1 hour after spinopelvic exercises same day.Spinopelvic parameter measurements on pre- and post-exercise radiographs including pelvic incidence, pelvic tilt, sacral slope and lumbar lordosis. All measurements are angles calculated in degrees.
Lumbar mobilityChange from baseline to up to 1 hour after spinopelvic exercises same dayCalculated as the change in angle of lumbar lordosis between neutral standing and flexed-forward seated radiographs.
Spinopelvic mobilityChange from baseline to up to 1 hour after spinopelvic exercises same dayCalculated as the change in angle of pelvic tilt between neutral standing and flexed-forward seated radiographs.
Patient risk classification for THA instabilityChange from baseline to up to 1 hour after spinopelvic exercises same dayRisk classification based on previously published risk factors for THA instability (lumbar stiffness, abnormal pelvic mobility, standing pelvic tilt greater than 13, sagittal spinal deformity)

Secondary

MeasureTime frameDescription
Use of medication for hip/back painBaselineAssessed by standard of care questionnaire prior to the pre-operative visit with provider for a total hip replacement.
Oswestry Disability Index scoreBaselinePatient reported outcome for pre-existing back pain and disability. The questionnaire is comprised of 10 sections, where each section is scored on a scale from 0 to 5 and summed. Higher score totals indicates worse disability.
Adverse eventsDay 1Any adverse events sustained from therapeutic exercises
Severity of hip arthritisBaselineGraded using Kellgren-Lawrence scale for osteoarthritis on AP radiographs. Grades are between 0-4, where 0 indicates an absence of osteoarthritis and a 4 indicates severe osteoarthritis.
Hip Society ScoreBaselinePatient reported outcome, scored from 0 to 100. Higher scores indicate better outcomes.
Hip disability and Osteoarthritis Outcome Score for Joint Replacement (HOOS, JR)BaselinePatient reported outcome, scored from 0 to 100. Higher scores indicate better outcomes.
The Veterans Rand 12-Item Health Survey scores (VR-12)BaselinePatient reported outcome. Scores are reported as a Z-score that is based on the United States population average of 50. Higher scores indicate better outcomes.

Contacts

Primary ContactMakenna Hemmerle, MS
makenna.hemmerle@adventhealth.com3032602951

Outcome results

None listed

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