Buerger's Exercises and Proprioceptive Drills on Postural Stability and Foot Perfusion in Elderly Patients With Chemotherapy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65+
SponsorSouth Valley University

About this trial

Chemotherapy-induced peripheral neuropathy (CIPN) is a common, dose-limiting side effect of neurotoxic chemotherapy agents, characterized by sensory loss, impaired proprioception, and muscle weakness, predominantly affecting the lower limbs. These impairments significantly contribute to postural instability and increase fall risk in elderly patients. Additionally, CIPN-associated microvascular changes can compromise peripheral circulation, further exacerbating neuromotor dysfunction and balance deficits.

While pharmacological options for CIPN are limited and often inadequate, exercise-based interventions have shown promise in mitigating functional impairments. Buerger's exercises, a vascular stimulation technique, are known to enhance peripheral blood flow, whereas proprioceptive drills can improve neuromuscular coordination and postural control. However, their combined effect on both postural stability and foot perfusion in elderly patients with CIPN has not been systematically studied.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Aged 65 years or older

Diagnosed with CIPN for at least 3 months

Demonstrating impaired postural stability (BBS ≤ 48 or ≥2 falls in the past year)

Medically cleared for exercise

Disqualifiers

Severe peripheral arterial disease (ABI < 0.5)

Severe postural hypotension or positional syncope

Recent orthopedic procedures or fractures (past 6 months)

Vestibular or cerebellar disorders

Trial design

Design model

Parallel

Treatments tested in this trial

  • Buerger's Exercises

    Combination product

    Buerger's Exercises + Proprioceptive Drills, 3 times/week for 8 weeks: * Buerger's Exercises: * Leg elevation at 45° for 2 min until blanching * Dependent sitting for 3 min until hyperemia * Supine rest for 5 min * 3 cycles per session * Proprioceptive Drills: * Single-leg stance * Tandem stance/walking * Heel-to-toe walking * Anterior-posterior and lateral weight shifts * Mini-squats on foam * Ankle alphabet * Progressively increased difficulty Sessions supervised by trained physiotherapists.

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: Intervention GroupExperimental treatment 1 intervention
Group B: Control GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Postural Stability Foot Perfusion

.Postural Stability: Overall Stability Index (OSI) via Biodex Balance System SD Foot Perfusion: Laser Doppler Flowmetry (LDF)

Time frame
Week 8
2

Pain scale (VAS) Quality of Life Index (QLI) - SCI Version

Pain scale (VAS) The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain." Quality of Life Index (QLI) - SCI Version Comprised of 4 domains: 1. Health and functioning 2. Psychological/spiritual 3. Social and economic 4. Family.

Time frame
8 weeks
3

Weight Height Body mass index

Weight in kg, height in meter and body mass index in kg/m2

Time frame
8 weeks

Secondary outcomes

1

Secondary Outcomes

* Berg Balance Scale (BBS) * Timed Up and Go Test (TUG) * Activities-specific Balance Confidence Scale * Number of falls Pain scale (VAS) Quality of Life Index (QLI) - SCI Version Follow-up (Week 8)

Time frame
8 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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

This trial is not recruiting at the moment. You can still explore other options: