Concurrent Training vs Soleus Push-Ups on Neurogenesis-Related Biomarkers in Diabetic Neuropathy Patients

Riphah International University

Status: Not yet enrolling

Conditions: Diabetic Peripheral Neuropathy Type 2

Treatments: Other: Concurrent Training; Other: Soleus Push-ups

Study type: Interventional

Funder types: Other

Identifiers

NCT07675720

RCRAHS-ISB/REC/PhD/011112

Details and patient eligibility

About

This study will examine how two types of exercise programs affect nerve health in people with diabetic peripheral neuropathy. Diabetic peripheral neuropathy is a common complication of type 2 diabetes that can cause numbness, pain, balance problems, and reduced quality of life. Exercise is often recommended for people with diabetes, but it is not yet clear which types of exercise are most effective for improving nerve function.

In this randomized controlled trial, participants with type 2 diabetes and confirmed peripheral neuropathy will be assigned to one of three groups. One group will perform a combined program of aerobic and resistance exercises (concurrent training). Another group will perform soleus push-up exercises, a seated ankle movement designed to activate the soleus muscle and improve glucose metabolism. The third group will continue with standard diabetes care and general lifestyle advice without a structured exercise program.

The study will evaluate whether these exercise interventions influence biological markers related to nerve repair and neuroplasticity, including brain-derived neurotrophic factor (BDNF), nerve growth factor (NGF), and the Schwann cell marker S100B. In addition, the study will assess changes in neuropathy symptoms, balance and postural stability, blood sugar control, and quality of life.

Participants will complete assessments before the intervention and again during follow-up after the exercise program. The findings of this study may help identify effective and feasible exercise strategies to support nerve health, improve physical function, and reduce the impact of diabetic peripheral neuropathy.

Enrollment: 99 estimated patients

Sex: All

Ages: 40 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 40-65 years
• Diagnosed Type 2 Diabetes Mellitus (T2DM) Confirmed diagnosis of T2DM for at least 5 years.
• Confirmed Diabetic Peripheral Neuropathy (DPN)

Diagnosis is based on clinical evaluation and scoring tools such as:

• Michigan Neuropathy Screening Instrument (MNSI) Cut-off value of ≥4 for Part A (History)(104) Cut-off value of ≥2 from Part B (Examination)(105)

• Vibration Pressure Threshold (≥25 Volts)(106)

  • HbA1c between 6.5% and 9.0% Reflecting moderate glycemic control, patients with extremely poor control were excluded for safety.
  • Stable medication regimen No changes in antidiabetic, antihypertensive, or neuropathy medications in the past 3 months.
  • Sedentary or low physical activity level Based on standard questionnaires (International Physical Activity Questionnaire - IPAQ), not currently engaged in structured exercise programs.
  • Ability to walk independently To ensure safety during aerobic or resistance exercise (for Group A).
  • Able to understand and follow instructions
  • Consent to participate and comply with study protocol
  • Written informed consent, obtained before randomization

Exclusion criteria

• History of recent cardiovascular events Includes myocardial infarction, stroke, or any cardiac intervention within the past 6 months.

  • Uncontrolled hypertension Blood pressure ≥160/100 mmHg at rest.
  • Severe musculoskeletal disorders or physical disability Including joint deformities, fractures, or amputation that limit the ability to perform exercise.
  • Severe diabetic foot ulcers or active lower limb infection Increases risk during lower limb activity or exercise.
  • End-stage renal disease (CKD stage 4 or higher) Associated systemic complications may confound study outcomes or affect safety.
  • Severe retinopathy or proliferative diabetic eye disease Exercise may pose risks such as retinal hemorrhage.
  • Current Smoker, tobacco or alcohol consumer. That may affect the blood biomarkers.
  • Cognitive impairment or psychiatric disorders That may affect understanding, compliance, or safety during exercise.
  • Participation in a structured exercise program within the last 3 months To avoid training-induced bias and ensure a sedentary baseline.
  • Chronic inflammatory or autoimmune conditions Conditions like rheumatoid arthritis or lupus may alter neurotrophic biomarkers.
  • Use of medications affecting neurogenesis or metabolism Such as corticosteroids, antipsychotics, or immunosuppressants.
  • Diagnosed sleep disorder
  • That may affect the outcomes of the intervention.
  • Pregnancy or lactation Due to altered physiology and ethical concerns.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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99 participants in 3 patient groups

Concurrent Training Group (CT)

Active Comparator group

Description:

Participants will undergo a combined aerobic and resistance exercise program.

Treatment:

Other: Concurrent Training

Soleus Push-Up Group (SPU)

Experimental group

Description:

Participants will perform seated plantar-flexion exercises targeting the soleus muscle, using a controlled movement protocol modeled after the soleus push-up method.

Treatment:

Other: Soleus Push-ups

Control Group

No Intervention group

Description:

Participants will receive standard diabetes care and general lifestyle advice without structured exercise intervention.