Information Needs, Preferences, and Understanding Trial (INPUT): A Randomized, Controlled Trial of the Effects of a Screening Tool on Illness Understanding

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This clinical trial compares the use of a new screening tool designed to evaluate patients' information needs, preferences, and illness understanding to the usual care to improve illness understanding in patients with lung cancer that has spread from where it first started (primary site) to other places in the body (metastatic) or for which no curative treatment is currently available (incurable). Goal concordant care is a model of care that aligns a patient's medical care with their values, preferences, and goals. Often, patients may not fully understand their illness and prognosis, but this information is important so that they can make fully informed decisions regarding their care that are consistent with their values, preferences, and goals. Completing the Information Needs, Preferences, and Understanding Trial (INPUT) screening tool may allow for more frequent and regular discussions regarding disease status and treatment goals, ultimately resulting in improved patient illness understanding and goal concordant care for patients with metastatic or incurable lung cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Within 3 months of biopsy-confirmed diagnosis of stage IV lung cancer

• Age 18 or over

• English speaking

• Attending a follow-up visit at the thoracic medical oncology clinic

• Plans to receive or actively undergoing cancer-directed systemic treatment at MD Anderson

Locations
United States
Texas
MD Anderson Cancer Center
RECRUITING
Houston
Contact Information
Primary
Kayley M Ancy, MD
kmclemings@mdanderson.org
832-729-1621
Time Frame
Start Date: 2024-12-16
Estimated Completion Date: 2027-12-31
Participants
Target number of participants: 100
Treatments
Active_comparator: Arm I (Standard care)
Patients undergo standard of care oncology follow-up visits.
Experimental: Arm II (INPUT screening)
Patients complete the INPUT screening tool at each of their standard of care follow up visits, with their medical oncology team.
Related Therapeutic Areas
Sponsors
Leads: M.D. Anderson Cancer Center

This content was sourced from clinicaltrials.gov

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