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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05694650
Other study ID # 2022-0654
Secondary ID NCI-2022-09841
Status Recruiting
Phase
First received
Last updated
Start date October 12, 2022
Est. completion date September 30, 2025

Study information

Verified date January 2024
Source M.D. Anderson Cancer Center
Contact Tacara Soones, MD, MPH
Phone (346) 720-7352
Email tnsoones@mdanderson.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of this qualitative research study is to assess the knowledge, attitudes and beliefs of cancer care providers, patients with cancer and caregivers regarding hospital care at home. We aim to conduct qualitative interviews to inform implementation of future on oncology hospital care at home programs


Description:

Interviews and focus groups will be conducted in English only using an interview guide (attached). The interview guide was based on the Consolidated Framework for Implementation Research (CFIR)8 to provide a broad understanding of the potential barriers and enablers of implementing a hospital care at home program. In summary, interviews will begin with an overview of the qualitative research study followed by verification of a completed demographic questionnaire


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date September 30, 2025
Est. primary completion date September 30, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Cancer Care Providers - Cancer care providers of any specialty, including but not limited to oncologists, surgeons, hospitalists, emergency medicine physicians, nurses (including nurse practitioners), physician assistants, and any other member of the cancer care team (eg social workers or physical therapists) - Employed by the University of Texas MD Anderson Cancer Center 2. Patients - Adults ages 18 and over - Currently undergoing or completed cancer treatment within the last 5 years at MD Anderson - Able to speak and read in English 3. Caregivers - Adults ages 18 and over - Self-identifies as a caregiver of an individual over 18 who is currently undergoing cancer treatment or completed cancer treatment within the last 5 years at MD Anderson - Able to speak and read in English Exclusion: None

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Focus Group
Participants can meet with an interviewer alone. The focus group should take about 1 hour and will be held in person at MD Anderson, by telephone, or online using a video conferencing app called Zoom
Interview
Participants can meet with an interviewer alone. The interview should take about 1 hour and will be held in person at MD Anderson, by telephone, or online using a video conferencing app called Zoom

Locations

Country Name City State
United States M D Anderson Cancer Center Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
M.D. Anderson Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of Life Questionnaires through study completion an average of 1 year
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