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 type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 27 (estimated) |
| Sponsor | Assaf-Harofeh Medical Center Government |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Tzrifin) |
| Status | Recruiting |
| Started | April 8, 2025 |
| Main results expected | December 11, 2027 |
| Study ends | December 11, 2027 |
| Registry record updated | September 4, 2026 |
| Trial ID | NCT06724861 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
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Shamir Medical center
Tzrifin, Israel Recruiting
Study contacts
- Study coordinator: Hadas Ofek, PT, PhD
- Email: hadasbarkolofek@gmail.com
- Phone: +972544666412
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Cryotherapy during weekly paclitaxel to reduce chemotherapy-induced numbness and tingling
This study tests whether applying cryotherapy to hands and feet during weekly paclitaxel helps prevent CIPN in women with breast cancer.
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Scrambler Therapy for chemotherapy-related nerve pain (CIPN).
Researchers will try Scrambler Therapy, a non-drug electrical treatment, to reduce pain and numbness in people with long-lasting chemotherapy-induced peripheral neuropathy.
-
VMD-3866 topical gel for chemotherapy-induced nerve pain
This trial will test whether a non-opioid topical gel called VMD-3866 can reduce pain in adults with chemotherapy-induced peripheral neuropathy.
-
Cryocompression to prevent taxane-induced nerve damage in the arms and legs.
This study tests whether cooling and pressure applied to the arms and legs during taxane chemotherapy can prevent or reduce numbness, pain, or weakness from peripheral neuropathy in adults with breast or gynecologic cancer.
-
SIR2501 plus Paclitaxel for solid tumors
This Phase 2 study tests SIR2501 in adults with solid tumors who are starting paclitaxel chemotherapy to see if it is safe and tolerable and to explore its effect on chemotherapy-induced neuropathy.
-
Non-invasive brain stimulation to help chemotherapy-induced nerve problems in cancer survivors
This trial tests whether a gentle brain stimulation method (tDCS) can help reduce numbness, tingling, and pain from CIPN in cancer survivors who are not currently in treatment.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.