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May 14, 2026PLoS ONE0 citationsOpen Access

Study protocol for a double-blinded randomized clinical trial evaluating effectiveness of neurodynamic approach in lower limb for diabetic peripheral sensory neuropathy

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AKAmbika KormokerKHK M Amran HossainMIMd. Shaharul Islam

Key Points

  • Evaluate the effectiveness of a neurodynamic approach with electrophysical stimulation in patients with diabetic peripheral sensory neuropathy.
  • 90 DPSN cases randomized into neurodynamic and sham approach groups
  • Each group receives transcutaneous electrical nerve stimulation and home exercises for 12 sessions over 4 weeks
  • Outcomes assessed with pretest, posttest, and follow-up evaluations.
  • Expected outcomes include reduced severity of neuropathic symptoms and improved quality of life.
  • Adverse events will be documented for safety analysis.

Abstract

Background Diabetic peripheral sensory neuropathy (DPSN) presents with pain or neuropathy symptoms and disturbances in lower limb sensory functions, leading to complicated diabetic foot conditions and declining quality of life. There is a research gap on the non-pharmacological conservative approach to this disabling condition. The objective of this study is to evaluate the effectiveness of the neurodynamic approach, along with electrophysical stimulation, in reducing the severity of neuropathic symptoms and improving the quality of life in patients with DPSN. Methods An assessor and patient-blinded randomized clinical trial (RCT) on 90 DPSN cases through hospital-based simple random sampling. Participants will be randomly assigned equally to either the Neurodynamic approach or the Sham neurodynamic approach group by concealed allocation between April and August 2025 at the Nurul Islam Diabetic Center in Jashore, Bangladesh. The experimental group will receive the Neurodynamic approach, and the control group will receive the sham approach; however, both groups will receive transcutaneous electrical nerve stimulation (TENS) and home exercises for 12 sessions over 4 weeks. A pretest will be taken at baseline, a posttest after 4 weeks, and a follow-up evaluation after 12 weeks. In addition to outcome measures, manageable and fatal adverse events will be documented and reported. Discussion This trial will be implemented in the non-pharmacological management of prevalent cases with DPSN and diabetic foot, sparing the burden of polypharmacy in people living with diabetes. Moreover, a positive result may guide clinicians toward an alternative in evidence-based practice, especially in a low-resource country like Bangladesh. This single-center trial may be limited by a lack of external generalizability, but it will lead to multicenter, large-sample studies in the future. Trial registration Registered from Clinical Trial Registry of India CTRI/2025/01/079801 Registered on: 30/01/2025 Trial Registered Prospectively.

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Cite This Study

Kormoker et al. (2026) studied this question.

synapsesocial.com/papers/6a0567a8a550a87e60a1fd82https://doi.org/10.1371/journal.pone.0348347
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