tSCS and AR Training on QoL and Physical Activity in Diabetic Neuropathy Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorRiphah International University

About this trial

Existing evidence of tSCS emphasizes pain relief and overlooks other functional parameters such as sensory enhancement, lower limb flexibility, and sustained improvements in physical activity and QoL.

Combined effects of tSCS and AR training on lower limb flexibility, vibration sense, QoL, and physical activity in patients with diabetic neuropathy. This dual approach has the potential to deliver a comprehensive strategy for managing DPN, which is low-cost, safe, and a more accessible solution for diabetic patients in Pakistan and around the world.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

More than or equals to 4 scores on Douleur Neuropathique 4 Questionnaire (DN4)

More than or equals to 6 Hz at Neurothesiometer

Disqualifiers

Cognitively compromised (MOCA score ≤ 26/30)

Metallic implants at skull

Shunting

Skin allergy

Trial design

Design model

Parallel

Treatments tested in this trial

  • Transcutaneous spinal cord stimulation Group

    Other intervention

    Transcutaneous spinal cord stimulation will be administered non-invasively using surface electrodes placed over the D12-L1 spinal segment. Stimulation will be delivered using the Soterix 1×1 Transcutaneous Electrical Stimulation (TES) unit. Stimulation will be applied at a frequency range of 30 Hz. The pulse duration is 1 ms, and the intensity will be set at 2 mA. A ramp-up and ramp-down time of 30 seconds will be used to enhance participant comfort during the start and end of each stimulation session, following standardized electrode placement and safety protocols. The stimulation will be delivered in a comfortable sitting or lying position

  • Augmented reality

    Other intervention

    AR-based rehabilitation will involve interactive balance and coordination tasks performed in a virtual environment all while receiving real-time visual feedback to guide movement accuracy and postural control. The main training block will comprise exercises focusing on hip flexion, hip abduction, knee flexion, and lateral weight shifting. Each module will be performed for 5-8 minutes, with short rest intervals between tasks.

Treatment groups

36 Participants
are divided into 3 treatment groups
Group A: Transcutaneous spinal cord stimulation + Augmented reality GroupExperimental treatment 2 interventions
Group B: Transcutaneous spinal cord stimulation GroupActive comparator 1 intervention
Group C: Augmented reality GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

International Physical Activity Questionnaire

The IPAQ assesses physical activity across four domains: work, transport, domestic, and recreation time. It includes 27 items and collects data on frequency and duration of physical activity at three intensity levels; high, moderate, and low. The IPAQ has Test-retest reliability ICC = 0.80. the score is calculated by converting activity into MET-minutes/week. Low activity: \< 600 MET-min/week, Moderate activity: 600-3000 MET-min/week and High activity: \> 3000 MET-min/week. Outcome will be measured at Baseline then Week 1 and then week 5

Time frame
Up to week 5
2

Diabetes Quality of Life Questionnaire

The Diabetes Quality of Life (D-QoL) questionnaire is a disease-specific instrument originally developed for the diabetes control and complications trial (DCCT) to assess the quality of life in individuals with diabetes mellitus. It has 46 items divided into three main domains: satisfaction, impact, and worry. Each item is rated on a likert scale, with higher scores indicating greater impact, or concern. The tool assesses the individual's perception of how diabetes affects various aspects of life, including daily activities, social functioning, and emotional well-being. The D-QoL has demonstrated strong reliability and validity, with internal consistency ranging from 0.73 to 0.94 for its subscales. Outcome will be measured at Baseline then Week 1 and then week 5

Time frame
Up to week 5

Secondary outcomes

1

Neurothesiometer

The neurothesiometer is a non-invasive and reliable device for assessing vibration perception threshold (VPT). The neurothesiometer demonstrated excellent intra-class correlation coefficients (ICCs) exceeding 0.90, highlighting its consistency. The cut off value of ≥ 6hz indicates presence of neuropathy. This tool is beneficial in clinical settings due to its ease of use, objective quantification, and ability to detect subclinical neuropathy. The neurothesiometer offers superior standardization, making it a preferred method for evaluating protective sensation and vibration loss in diabetic populations. Outcome will be measured at Baseline then Week 1 and then week 5

Time frame
Up to week 5
2

Sit and reach test

The sit-and-reach test is a widely used tool for assessing lower limb flexibility. The test demonstrates excellent reliability, with intra-class correlation coefficients (ICCs) ranging from 0.92 to 0.99, indicating strong consistency in repeated measures. Scoring is based on distances recorded in inches or centimeters, higher values indicate better flexibility. It is simple to administer, cost-effective, making it a reliable method for flexibility assessment in healthy adult populations. Outcome will be measured at Baseline then Week 1 and then week 5

Time frame
Up to week 5

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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