Spastic Paraplegia Type 7 Clinical Trials

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Noninvasive Spinal Cord Neuromodulation to Enhance Motor Function in Individuals With Hereditary Spastic Paraplegia

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Hereditary spastic paraplegia (HSP) is a rare neurological condition that causes stiffness, weakness, and difficulty walking due to damage in the nerves that control movement. This study will test whether a noninvasive form of spinal cord stimulation, called transcutaneous spinal cord stimulation (tSCS), can improve walking and reduce muscle stiffness in adults with HSP. In this study, participants will receive tSCS twice a week for 8 weeks. The stimulation is delivered through self-adhesive electrodes placed on the skin over the lower back and does not require surgery. Each session will last about one hour. After the treatment period, participants will be followed for an additional 8 weeks without stimulation to see whether any improvements are maintained. Researchers will measure walking speed, walking endurance, muscle stiffness, and overall disease severity. Additional tests will explore changes in bladder and bowel function and muscle strength.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Clinical diagnosis of hereditary spastic paraplegia (genetic confirmation if available).

• Stable medications for spasticity and other neurologic symptoms for =4 weeks prior to enrollment.

• Able to participate in study visits and assessments with or without assistive devices.

• If ambulatory: able to walk at least 10 meters with or without an assistive device.

• If wheelchair user: able to perform seated mobility tasks and transfers required for assessments.

• Capacity to provide informed consent and follow study procedures, with an ability to communicate and understand instructions in English

Locations
United States
Kentucky
University of Kentucky
RECRUITING
Lexington
Contact Information
Primary
Rahul Sachdeva, PhD
rahulsachdeva@uky.edu
8592574888
Time Frame
Start Date: 2026-03-01
Estimated Completion Date: 2028-02-01
Participants
Target number of participants: 15
Treatments
Experimental: Participants with Hereditary Spastic Paraplegia
Participants will undergo 16 transcutaneous spinal cord stimulation (tSCS) sessions over 8 weeks
Sponsors
Collaborators: Spastic Paraplegia Foundation
Leads: Rahul Sachdeva

This content was sourced from clinicaltrials.gov