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NCT05995860Completed

Study of a Rapid Triadic Communication Intention Elicitation Intervention to Improve Supportive Oncology Care Delivery

Pilot Study of a Rapid Triadic Communication Intention Elicitation Intervention (PRECursOr) to Improve Supportive Oncology Care Delivery for Patients With Advanced, Incurable Cancer and Their Caregivers

Source: ClinicalTrials.gov · Last updated 28 Jan 2025

Brief summary (registry, in English)

The purpose of this study is to help test an idea designed to foster more supportive talk between providers (doctors or nurse practitioners), patients, and caregivers during an outpatient oncology appointment. A caregiver is the person the patient identifies is primarily involved in their healthcare. This study is collecting your reaction to this idea in order to understand needed changes before we introduce the idea to a larger group of patients.

Status (registry)
Completed
Study type
Interventional
Enrollment
47 (actual)
First submitted
10 Jul 2023
Start date
14 Jun 2023
Primary completion date
9 Jan 2025
Lead sponsor
Indiana University
NCT number
NCT05995860

What you commit to

  • Study type: Interventional
  • Participants enrolled: 47
  • From 14 Jun 2023 to the primary completion date, 9 Jan 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • cognitive impairment, or

Other

  • patients and/or caregivers will be excluded if either one or both demonstrate:
  • speech/hearing difficulties precluding participation.

Who the study is looking for

  • patients will:
    • be adult women with an incurable gynecologic cancer (i.e., evidence of refractory/progressive disease after first-line treatment or recurrent disease),
    • not be receiving specialty palliative care or hospice,
    • read/speak English, and
    • be able to provide written informed consent.
  • caregivers will:
    • identify as the individual who is primarily involved in the patient's care,
    • be able to attend the oncology encounter,
    • read/speak English, and
    • be able to provide written informed consent.
  • providers will:
    • specialize in gynecologic oncology, and
    • provide outpatient care at IUSCCC gynecologic oncology clinic.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
IU Health Joe and Shelly Schwarz Cancer Center
Coordinator of this site? Confirm its status
CarmelUnited StatesUnknown status
Indiana University Melvin and Bren Simon Comprehensive Cancer Center
Coordinator of this site? Confirm its status
IndianapolisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.