Neuromodulation to Enhance Motor Function in HSP

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorRahul Sachdeva

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

Implanted electronic devices (e.g., pacemaker, deep brain stimulator, intrathecal pumps).

Severe cardiopulmonary disease that would make participation unsafe.

Open skin lesions or severe dermatologic conditions at electrode sites.

Pregnancy or plans to become pregnant during the intervention period.

Trial design

Design model

Single group

Treatments tested in this trial

  • transcutaneous spinal cord stimulation

    Device

    a non-invasive spinal neuromodulation system will deliver stimulation as high-frequency pulsed current using frequencies within a predefined range

Treatment groups

15 Participants
are divided into 1 treatment group
Group A: Participants with Hereditary Spastic ParaplegiaExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Change in 10-Meter Walk Test (10MWT)

10MWT assesses walking speed over a 10-meter walkway at a comfortable and maximum safe pace. Timing occurs between 2 and 8 meters to exclude acceleration/deceleration, with two trials averaged per speed. Assistive devices are allowed

Time frame
Baseline, Weeks 1, 4, 8, and 16
2

Change in 6- Minute Walk Test (6MWT)

6MWT evaluates walking endurance by measuring the total distance walked over six minutes. Patients are instructed to walk as far as possible at their own pace, with rests allowed if needed. The total distance reflects functional capacity and stamina, which are often affected in HSP due to progressive spasticity and weakness.

Time frame
Baseline, Weeks 1, 4, 8 and 16
3

Change in Modified Ashworth Scale (MAS)

measures muscle spasticity by assessing resistance to passive muscle stretch through the range of motion and grades the muscle tone on a 0-4 scale based on the resistance felt. MAS 0-4 scale: 0: No increased muscle tone 1: Slight increase in tone; catch and release at the end of the range 1+ : Slight increase; catch followed by minimal resistance through \< half the range 2: More marked increase through most of the range, but the limb still moves easily 3: Considerable increase in tone; passive movement is difficult 4: Limb is rigid in flexion or extension

Time frame
Baseline, Weeks 1, 4, 8, and 16
4

Change in Spastic Paraplegia Rating Scale (SPRS)

The Spastic Paraplegia Rating Scale (SPRS) is a validated clinical outcome measure used to assess disease severity in individuals with spastic paraplegia. The scale consists of 13 items evaluating gait, spasticity, muscle strength, coordination, and functional impairment. Each item is scored to yield a total score ranging from 0 to 52, where a score of 0 indicates no neurological disability and higher scores reflect increasing severity of impairment, with 52 representing the most severe disease manifestation.

Time frame
Baseline, Weeks 1, 4, 8, and 16

Secondary outcomes

1

Change in HSP- Self Notion and Perception (HSP-SNAP) questionnaire

HSP-SNAP is a questionnaire used to assess the self-perception of individuals diagnosed with hereditary spastic paraplegia (HSP). HSP-SNAP includes 12 questions, with 2 items dedicated to each symptom dimension (stiffness, weakness, imbalance, reduced endurance, fatigue, and pain). Each pair of items for a given dimension includes both positive and negative responses to prevent automatic answers. The HSP-SNAP employs a 5-point Likert scale (1 = strongly disagree, 2 = disagree, 3 = neutral, 4 = agree, 5 = strongly agree). To account for both positive and negative items, scoring is as follows: for items with a positive tone, the score is calculated as "patient's score minus 1" (pt score-1); for negative items, the score is "5 minus the patient's score" (5-pt score). The overall score is the sum of all item scores, ranging from 0 to 48. A higher score indicates better well-being and milder symptoms.

Time frame
Baseline, Weeks 1, 4, 8, and 16
2

Change in Joint Kinematics via Three-dimensional (3D) gait analysis

3D Gait Analysis will be performed using a 14-camera motion capture system, a wireless Electromyography (EMG) system, and 3 in-ground force plates. We will track walking speed using timing gates. Wireless EMG sensors will be placed on the vastus lateralis, rectus femoris, and vastus medialis to assess muscle activation during the gait trials. The outcomes will include joint kinematics (hip, knee, and ankle,).

Time frame
Baseline, Weeks 1, 4, 8, and 16
3

Change in Sit-to-stand test

Participants will be asked to perform a sit-to-stand task, whereby they will be told to stand up and sit down on a stool at their own self-selected pace. Sit-to-Stand performance, measured as the time and kinematic characteristics of sit-to-stand transition (average of two trials) obtained using motion capture analysis.

Time frame
Baseline, Weeks 1, 4, 8, and 16
4

Change in Bilateral isometric knee strength

Bilateral isometric knee strength will be obtained with three, 5-sec maximal voluntary isometric contractions (MVIC) separated by one-minute rest. Knee strength, measured as peak knee extensor torque obtained using isokinetic dynamometry (Biodex), expressed in Newton-meters (Nm), with higher values indicating greater muscle strength.

Time frame
Baseline, Weeks 1, 4, 8, and 16

Other outcomes

1

Change in Neurogenic Bladder Symptom Score (NBSS)

The Neurogenic Bladder Symptom Score (NBSS) is a validated, disease-specific patient-reported outcome measure designed to assess lower urinary tract symptoms in individuals with neurogenic bladder. The questionnaire evaluates symptom severity across three domains, including incontinence, storage and voiding symptoms, and bladder-related consequences, as well as a global quality-of-life item. Individual items are scored on ordinal response scales, and summed to generate a total score ranging from 0 to 74, with higher scores indicating greater urinary symptom severity and impact on daily functioning.

Time frame
Baseline, Weeks 1, 4, 8, and 16
2

Change in Neurogenic bowel dysfunction score (NBD Score)

The Neurogenic Bowel Dysfunction Score (NBDS) is a validated clinical questionnaire used to assess the severity and impact of bowel dysfunction in individuals with neurological conditions, including spinal cord injury. The instrument evaluates multiple domains of bowel function, including frequency of defecation, constipation, fecal incontinence, use of medication or mechanical assistance, and impact on quality of life. Individual item scores are summed to yield a total score ranging from 0 to 47, with higher scores indicating more severe bowel dysfunction and greater impact on daily living.

Time frame
Baseline, Weeks 1, 4, 8, and 16.
3

Change in Metabolic/protein profiling

Approximately 10 mL of venous blood samples will be collected and processed for metabolomic/lipid profiling and biomarker assays

Time frame
Baseline, Weeks 1, 4, 8, and 16

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Rahul Sachdeva

Lead sponsor

University of Kentucky

Sponsor institution

Spastic Paraplegia Foundation

Collaborator