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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04266522
Other study ID # 2019-104
Secondary ID P30CA022453
Status Completed
Phase N/A
First received
Last updated
Start date January 16, 2020
Est. completion date September 30, 2021

Study information

Verified date October 2022
Source Barbara Ann Karmanos Cancer Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This phase II trial studies how well medical physics direct patient care works in improving patients' understanding of their cancer treatment. Providing direct physicist-patient interactions and answering patients' questions about their cancer treatment may help patients to understand the care and therefore reduce anxiety and distress during treatment.


Description:

PRIMARY OBJECTIVE: I. To evaluate whether the Medical Physics Direct Patient Care Initiative (MPDPCI) improves anxiety/distress. SECONDARY OBJECTIVE: II. To assess whether the MPDPCI improves patient treatment adherence and overall satisfaction. OUTLINE: Patients are randomized to 1 of 2 arms. ARM I: Patients receive printed materials describing the technical aspects of their treatment. ARM II: Patients receive printed materials as in Arm I. Patients also receive a minimum of 2 direct physicist interactions to describe the technical aspects of their treatment either immediately prior to or immediately after treatment simulation.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date September 30, 2021
Est. primary completion date September 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Medical physicists will be eligible if they care for patients within the Gershenson Radiation Oncology Center within the Karmanos Cancer Institute and have completed the patient communication training - Are able to read and write in English - Are scheduled for curative radiation therapy at the Gershenson Radiation Oncology Center Exclusion Criteria: - NONE

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Informational Intervention
Receive printed materials
Counseling
Receive direct physicist interactions to describe the technical aspects of the treatment
Questionnaire Administration
Ancillary studies

Locations

Country Name City State
United States Barbara Ann Karmanos Cancer Institute Detroit Michigan

Sponsors (2)

Lead Sponsor Collaborator
Barbara Ann Karmanos Cancer Institute National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anxiety Will be assessed using linear mixed-effects models. These objectives will be evaluated based on the difference between groups across three time points (i.e., group-effect) using the baseline corrected measurements. Each patient will be considered as random-effects along with the repeated measurements at three time points. The repeated measurements at three time points will be handled by autocorrelated residuals within groups. 4 months
Primary Distress Will be assessed using linear mixed-effects models. These objectives will be evaluated based on the difference between groups across three time points (i.e., group-effect) using the baseline corrected measurements. Each patient will be considered as random-effects along with the repeated measurements at three time points. The repeated measurements at three time points will be handled by autocorrelated residuals within groups. 4 months
Secondary Patient treatment adherence Will be assessed using 2-sided unpaired t-test. 4 months
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