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NCT05496972 Clinical Trial

Survey Assessment of Patient and Provider Impressions of Telemedicine in Radiation Oncology

Malignant Solid Neoplasm Clinical Trial

Official title:
Survey Assessment of Patient and Provider Impressions of Telemedicine in Radiation Oncology

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT05496972
Other study ID # 2020-1063
Secondary ID NCI-2021-09908
Status Active, not recruiting
Phase
First received
Last updated
Start date April 21, 2021
Est. completion date July 1, 2027

Study information
Verified date June 2024
Source M.D. Anderson Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To understand more about the opinions of patients and health providers on the use of telemedicine in radiation oncology.

Description:

Primary Objective: To characterize patient and provider satisfaction with telemedicine in RO Secondary Objective: - To provide evidence for or against the use of telemedicine in radiation oncology (RO) - To assess the feasibility of and value added by telemedicine in RO - To describe barriers and facilitators to telemedicine in RO - To identify preferred use cases for telemedicine in RO

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 200
Est. completion date July 1, 2027
Est. primary completion date July 1, 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients will be eligible if they are aged 18 or older and have undergone at least 1 telemedicine encounter (video visit) with the radiation oncology department at MD Anderson or its affiliates within 2 months from the initiation of the study (and prospectively as the study enrolls). This would include weekly see visits, follow-up visits, or consultations - English speaking - Access to email and internet to complete the survey - Attending physicians in the radiation oncology department who have utilized telemedicine will be contacted to fill out surveys reflecting their experience Exclusion Criteria: • Protected populations such as adults unable to consent, pregnant women, prisoners, and individuals who are not yet adults will be excluded

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Survey Administration
Patients and providers complete survey over 10 minutes about their perspectives on the use of telemedicine

Locations
Country Name City State
United States MD 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 Patient satisfaction survey with telemedicine in radiation oncology (RO) Sensitivity analyses will be performed with those rating 9 or higher or less than 9, and for those who "agree" or "strongly agree" with whether they are satisfied with telemedicine compared to those who give other answers. through study completion and average of one year.
Primary Provider satisfaction survey with telemedicine in radiation oncology (RO) Sensitivity analyses will be performed with those rating 9 or higher or less than 9, and for those who "agree" or "strongly agree" with whether they are satisfied with telemedicine compared to those who give other answers. through study completion and average of one year.
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