Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Explicit Sensory Retraining for Chemo-Induced Peripheral Neuropathy

Official title: Sensory Rehabilitation in CIPN

Run by Assaf-Harofeh Medical Center · NCT06724861 · Data updated 2026-11-12

This study tests whether three sessions of explicit sensory retraining for the legs, compared with usual care, can help reduce symptoms and improve function in adults with CIPN after chemotherapy.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment27 (estimated)
SponsorAssaf-Harofeh Medical Center
Government
Drugs / interventionschemotherapy
Locations1 site (Tzrifin)
StatusRecruiting
StartedApril 8, 2025
Main results expectedDecember 11, 2027
Study endsDecember 11, 2027
Registry record updatedSeptember 4, 2026
Trial IDNCT06724861 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults over 18 with CIPN lasting at least 3 months after chemotherapy, able to walk prior to chemotherapy, and proficient in the questionnaire language.

Probably not a fit

Individuals with pre-chemotherapy neuropathy, significant CNS involvement, or those not ambulatory before chemotherapy may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This cross-over randomized trial evaluates the effect of explicit sensory retraining for the lower extremities in adults with chemotherapy-induced peripheral neuropathy. Participants receive three sessions, each spaced about a week apart, and outcomes include subjective symptom scores, pain, mobility, balance, sensory thresholds, and proprioception. The study uses measures such as TNAS, VAS, TUG, FABS, monofilament touch testing, and a home exercise log. CIPN is a common, long-lasting complication of chemotherapy that can impair function and quality of life, especially in sensory fibers of the feet and legs. Active sensory rehabilitation has shown benefit in other neurological conditions, and this trial investigates its applicability to CIPN.

Why it matters

Potential benefit: If successful, participants may experience reduced neuropathic symptoms and improved balance and mobility.

How similar studies have gone: Previous work in other neurologic conditions suggests sensory retraining can improve sensation and function; CIPN-specific data are limited, making this investigation noteworthy.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* CIPN by self-report (present or absent) \> 3 months after last chemotherapy treatment
* age \> 18.

Exclusion Criteria:

* Pre-chemotherapy neuropathy/ sensory impairment
* recurrent falls prior to chemotherapy (more than 2 per year)
* CNS involvement
* not ambulatory before chemotherapy
* Hebrew proficiency not meeting questionnaires' needs.

Where it's running

  • Shamir Medical center
    Tzrifin, Israel
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.