M D Anderson Cancer Center
Houston, Texas, 77030, United States
Location status: Recruiting
Location contact
Barbara J O'Brien, MD
CONTACT
Barbara J O'Brien, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT04988009
This study evaluates patient perceptions around quality of care through telemedicine in neuro-oncology. Studying questionnaires related to perceptions quality of care through telemedicine in patients with brain cancer may help doctors to improve the delivery of care through this modality.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Houston, Texas, 77030, United States
Location status: Recruiting
Barbara J O'Brien, MD
CONTACT
Barbara J O'Brien, MD
PRINCIPAL_INVESTIGATOR
PRIMARY OBJECTIVE:
I. To evaluate the patient-perceived quality of care by group (telemedicine versus in-person visits) in patients with central nervous system (CNS) cancer.
SECONDARY OBJECTIVES:
I. To characterize the visits provided by telemedicine compared to those in-person.
II. To contrast the average time spent on telemedicine visits compared to in-person visits, and the delay between visit order placement and visit occurring.
III. To evaluate the domains of patient care addressed on a telemedicine visit versus in-person visit per documentation, including (1) treatment planning, (2) symptom burden, (3) goals of care.
IV. To evaluate frequency of acute care sought (through emergency room or urgent care clinic) within 30 days of encounter in telemedicine visit versus (vs) in-person visit.
V. The impact of patient and clinical characteristics on perceived quality of care in the context of covariate-adjusted modeling.
OUTLINE:
Patients complete a survey related to their perceived quality of care via telephone and have their medical chart reviewed prospectively.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Review of medical chart
Complete survey
Time frame: through study completion, an average of 1 year
Survey responses will be summarized by ordinal category as counts with percentages, separately by group. Will separately estimate the proportion of each ordinal level of each group with 95% confidence interval.
Time frame: through study completion, an average of 1 year
Will separately estimate the proportion of each ordinal level of each group with 95% confidence interval.
Time frame: Baseline
Differences between groups will be assessed by 2-sample 2-sided t-test and Mann-Whitney test, Fisher's exact test, or chi-square test.
Time frame: through study completion, an average of 1 year
Will be summarized by group per mean, median, standard deviation, and range. Differences between groups will be assessed by t-test and Mann-Whitney test.
Time frame: through study completion, an average of 1 year
Will be summarized by group per mean, median, standard deviation, and range. Differences between groups will be assessed by t-test and Mann-Whitney test.
Time frame: through study completion, an average of 1 year
Will be summarized as counts with percentages by group. Differences between groups will be assessed by chi-square test.
Time frame: Within 30 days of encounter
Will be summarized as counts with percentages by group. Differences between groups will be provisionally assessed by Fisher's exact test.
Contact information is provided by the study sponsor or research team.
M.D. Anderson Cancer Center
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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