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NCT06736600 · ClinicalTrials.gov registry record · NA

Patient-identified Values as Outcome Targets (PIVOT) Feasibility Pilot Trial

A NA study of Peripheral Neuropathy Due to Chemotherapy, sponsored by M.D. Anderson Cancer Center.

Recruiting
Registry status
NA
Development phase
45
Enrollment target
1
Study location

NCT06736600: Recruiting NA study of Peripheral Neuropathy Due to Chemotherapy, sponsored by M.D. Anderson Cancer Center.

NCT06736600 is a NA study of Peripheral Neuropathy Due to Chemotherapy that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 45 participants, below the 54-participant average among 6 other Peripheral Neuropathy Due to Chemotherapy trials with a reported enrollment target (17% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06736600, a NA study of Peripheral Neuropathy Due to Chemotherapy, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

RECRUITING
Registry status
NA
Development phase
45 participants
Enrollment target
1
Study location

Study Summary

A behavioral trial aimed at helping patients identify what matters most to them and is part of a larger effort to pivot from disease-oriented care to whole-person care.

Primary Outcome

Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0

Interventions

  • BEHAVIORAL Goal Attainment Scaling (GAS)

Study Locations (1)

Texas

  • The University of Texas M. D. Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 45 participants
Start Date 2025-04-18
Est. Completion 2027-08-31
Phase NA
M.D. Anderson Cancer Center

2,692 total trials

What NCT06736600 shows while recruiting

NCT06736600 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 45 participants, a relatively small participant target, below the 54-participant average among 6 other Peripheral Neuropathy Due to Chemotherapy trials with a reported enrollment target (17% lower).

The record links to 1 condition, with Peripheral Neuropathy Due to Chemotherapy appearing as the primary indexed condition, and to 1 intervention - of which Goal Attainment Scaling (GAS) is the first listed.

NCT06736600 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT06736600 about?

NCT06736600 is a clinical study titled "Patient-identified Values as Outcome Targets (PIVOT) Feasibility Pilot Trial". A behavioral trial aimed at helping patients identify what matters most to them and is part of a larger effort to pivot from disease-oriented care to whole-person care.

What is the current status of trial NCT06736600?

This trial is currently recruiting. It is a NA study. The enrollment target is 45 participants. The study started on 2025-04-18. Estimated completion is 2027-08-31.

What conditions does trial NCT06736600 study?

This clinical trial studies the following conditions: Peripheral Neuropathy Due to Chemotherapy.

What interventions are being tested in trial NCT06736600?

The interventions under investigation include: Goal Attainment Scaling (GAS) (BEHAVIORAL).

Who is sponsoring clinical trial NCT06736600?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06736600 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT06736600, the US trial registry maintained by the National Library of Medicine. NCT06736600 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.