RecruitingNot ApplicableNCT06736600

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


Sponsor

M.D. Anderson Cancer Center

Enrollment

45 participants

Start Date

Apr 18, 2025

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Inclusion Criteria11

  • Provision of signed and dated electronic informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Age 18 or older.
  • Documented diagnosis of chemotherapy-induced peripheral neuropathy meeting the following criteria: 1) onset associated with timing of neurotoxic chemotherapy and 2) symptomatic reports of peripheral neuropathy.
  • Access to smartphone and internet for participating in a technology-based intervention
  • Upcoming in-person appointment in the Main Hospital Pain Management Clinic 4-6 weeks from the consent date.
  • English-speaking
  • Pain or bothersome symptoms present most days of the week at an average of ≥4/10 on the Numeric Rating Scale for the past 3 months
  • No longer receiving cancer treatment or has been on stable maintenance treatment for the past 3 months.
  • Resides in the Houston Metroplex
  • A score ≤7 on the validated Six Item Cognitive Impairment Test (6CIT) for unimpaired cognition

Exclusion Criteria11

  • Provision of signed and dated electronic informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Age 18 or older.
  • Documented diagnosis of chemotherapy-induced peripheral neuropathy meeting the following criteria: 1) onset associated with timing of neurotoxic chemotherapy and 2) symptomatic reports of peripheral neuropathy.
  • Access to smartphone and internet for participating in a technology-based intervention
  • Upcoming in-person appointment in the Main Hospital Pain Management Clinic 4-6 weeks from the consent date.
  • English-speaking
  • Pain or bothersome symptoms present most days of the week at an average of ≥4/10 on the Numeric Rating Scale for the past 3 months
  • No longer receiving cancer treatment or has been on stable maintenance treatment for the past 3 months.
  • Resides in the Houston Metroplex
  • A score ≤7 on the validated Six Item Cognitive Impairment Test (6CIT) for unimpaired cognition

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Interventions

BEHAVIORALGoal Attainment Scaling (GAS)

Goal-setting tele-coaching and the well-studied Patient Priorities Care framework will assist participants with bothersome CIPN identify their most important health goals and scale them into specific, measurable, achievable, relevant, and time-bound (SMART) goals


Locations(1)

The University of Texas M. D. Anderson Cancer Center

Houston, Texas, United States

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NCT06736600


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