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RECRUITING
NCT06666608
NA

Bone Stimulator for Spondylolysis

Sponsor: The Methodist Hospital Research Institute

View on ClinicalTrials.gov

Summary

This prospective study aims to investigate the effectiveness of bone stimulator therapy as adjunct treatment of spondylolysis in athletic populations. By evaluating its impact on pain reduction, functional improvement, osseous bony union and return-to-sport time, the investigators seek to provide valuable insights into the role of bone stimulation therapy as a potential treatment modality for this challenging condition.

Official title: The Efficacy of Bone Stimulator in Treatment and Return-to-Sport for Spondylolysis

Key Details

Gender

All

Age Range

16 Years - 40 Years

Study Type

INTERVENTIONAL

Enrollment

48

Start Date

2025-12-03

Completion Date

2029-12

Last Updated

2026-03-25

Healthy Volunteers

No

Interventions

DEVICE

Bone Stimulator

Subjects will be asked to wear their device (if applicable) for a minimum of 30 minutes a day for 12 weeks with no maximum usage time. The device will track compliance. Bone stimulator should be worn at rest.

OTHER

Standard of Care Spondylolysis Treatment

Participants will follow the standard of care regimen for spondylolysis treatment at Houston Methodist which will involve physical therapy and wearing a back brace.

Locations (1)

Houston Methodist Hospital

Houston, Texas, United States