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The Effectiveness of Anti-Gravity Treadmill Training

The Effectiveness of Anti-Gravity Treadmill Training in Patients After Lumbar Microdiscectomy and Fusion Surgeries

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01689922
Enrollment
27
Registered
2012-09-21
Start date
2012-06-30
Completion date
2016-08-31
Last updated
2017-03-01

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

Conditions

Lumbar Degenerative Disc Disease

Brief summary

The primary objective of this study is to compare the effectiveness of standard for our practice postoperative physical therapy (PT) program to a PT program that incorporates lower body positive pressure (LBPP) treadmill training for the patients after lumbar discectomy and fusion surgeries.

Detailed description

A prospective, randomized, parallel group controlled clinical study is proposed. The patients will be divided into the two study groups according to the surgical procedure: 1. patients undergoing one-level microdiscectomy for lumbar herniated disc 2. patients undergoing one-level lumbar fusion for degenerative disc disease without notable spinal stenosis. Each group will consist of 60 patients (see sample size calculations below) who will be randomized into the two equal groups to undergo: 1. Standard postoperative rehabilitation program 2. Standard postoperative rehabilitation program with addition of lower body positive pressure (LBPP) treadmill training

Interventions

OTHERAlterG

All patients will begin an early postoperative rehabilitation program and standard PT no later than 4 weeks following surgery and continue for at least 6 weeks. The duration of standard PT program could be extended depending on the patient needs. The patients randomized to undergo (LBPP) treadmill training will have an additional 7-week 3 times a week training on the antigravity

Sponsors

Justin Parker Neurological Institute
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Adults between 18 and 65 years old * Willing and able to comply with protocol and PT requirements * Patients with primarily radicular and back pain due to degenerative disc disease requiring one-level discectomy for herniated disc or lumbar fusion between L2 and S1 * Willing and able to sign a study specific informed consent

Exclusion criteria

* Require more than one-level surgery * No previous lumbar surgery * Any ongoing health condition that would make it difficult to adhere to postoperative PT requirements * Peri-operative or post-operative complications (infection, pneumonia, nerve injury, dural tear, etc.) that would constraint or delay the ability to participate in postoperative PT * BMI greater than 40 * Active local or systemic infection

Design outcomes

Primary

MeasureTime frameDescription
Oswestry Disability Questionnaire24 months10 points or 20% improvement on Oswestry Disability Questionnaire

Secondary

MeasureTime frame
Patient Global Outcome Ratings and Health Quality Improvement24 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026