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OTHERClinicalTrials.govClinical trialNot applicableEnrolling by invitation

Effectiveness of Video-Based Movement Analysis-Guided Personalized Rehabilitation in Patients With Chemotherapy-Induced Peripheral Neuropathy (CIPN)

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Official record

Identifier
NCT07714278
Recruiting locations

country

South Korea
Interventions studied
ReMapUsual Care
Lead sponsor
Seoul National University Bundang Hospital
Target enrolment
150 participants
Study type
INTERVENTIONAL
Phase
Not applicable
Status
Enrolling by invitation
First posted
Jul 20, 2026
Last updated on the registry
Aug 14, 2026
Age
19 Years
Sex
ALL
Study contact
No public contact is listed on the official record.
Eligibility criteria

Reproduced verbatim from the official record. Eligibility is decided by the study team, never by this page.

Inclusion Criteria:

* Adult patients aged 19 years or older.
* Diagnosed with breast cancer, colorectal cancer, or gynecological cancer, and currently receiving chemotherapy or under follow-up observation after completing treatment.
* History of treatment with neurotoxic chemotherapeutic agents (e.g., taxane, platinum, etc.) or experiencing related symptoms.
* Symptoms or risk of chemotherapy-induced peripheral neuropathy (CIPN) (NCI-CTCAE Grade \>= 1).
* Able to walk independently (with or without assistive devices).
* Able to understand the study purpose and procedures and voluntarily provide written informed consent.

Exclusion Criteria:

* Peripheral neuropathy clearly attributable to causes other than CIPN, such as diabetic neuropathy.
* Severe central nervous system disorders (e.g., stroke, Parkinson's disease, etc.) or severe musculoskeletal disorders that make functional assessment or exercise performance difficult.
* Severe cognitive impairment that interferes with study participation or the ability to follow instructions.
* Recent significant injury due to a fall, or cases where exercise performance is deemed medically unsafe.
* Recurrent or progressive cancer with an unstable general systemic condition.
* Any other condition or clinical reason that, in the opinion of the investigator, makes participation in the study inappropriate.
Indexed under
Breast Cancer