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

Sponsor
M.D. Anderson Cancer Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT05496972
Collaborator
(none)
200
1
20.3
9.8

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Survey Administration

Detailed 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

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Survey Assessment of Patient and Provider Impressions of Telemedicine in Radiation Oncology
Actual Study Start Date :
Apr 21, 2021
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Telemedicine Visits

Participants are asked to fill out a survey about their experience.

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

Outcome Measures

Primary Outcome Measures

  1. Patient satisfaction survey with telemedicine in radiation oncology (RO) [through study completion and average of one year.]

    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.

  2. Provider satisfaction survey with telemedicine in radiation oncology (RO) [through study completion and average of one year.]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 MD Anderson Cancer Center Houston Texas United States 77030

Sponsors and Collaborators

  • M.D. Anderson Cancer Center

Investigators

  • Principal Investigator: Chenyang Wang, MD, M.D. Anderson Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier:
NCT05496972
Other Study ID Numbers:
  • 2020-1063
  • NCI-2021-09908
First Posted:
Aug 11, 2022
Last Update Posted:
Aug 18, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 18, 2022