Ignite Creation Date:
2024-05-06 @ 3:26 PM
Last Modification Date:
2024-10-26 @ 1:49 PM
Study NCT ID:
NCT04633616
Status:
COMPLETED
Last Update Posted:
2022-12-15
First Post:
2020-11-06
Brief Title:
Tailored Patient-Provider Communication TPPC Evaluating the Impact of TPPC in Dermatology Patients
Sponsor:
University of Southern California
Organization:
University of Southern California
Study Overview
Official Title:
Tailored Patient-Provider Communication TPPC A Pragmatic Single-Blinded Trial Evaluating the Impact of TPPC in Dermatology Patients Compared to Standard Patient-Provider Communication
Status:
COMPLETED
Status Verified Date:
2022-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The impact of tailored patient-provider communication to improve clinical trial recruitment patient knowledge and patient engagement will be studied Tailored patient-provider communication refers to the individualization of patient-provider communication using patients preferred methods of communication This involves the utilization of social messaging such as e-mail or text andor social media platforms These communication methods purport to and meet individual patient needs whilst ensuring that information is received and in a format that is familiar to each patient The primary outcomes of the proposed research is to evaluate the impact of tailored patient-provider communication on patient response rates speed and number clinical trial recruitment rates patient knowledge and patient engagement
Detailed Description:
This is a 3-month pragmatic single-blinded randomized controlled trial evaluating the impact of tailored patient-provider communication on patient engagement and clinical outcomes of adult dermatology patients compared to non-tailored patient-provider communication The pragmatic trial will compare patient engagement and clinical outcomes between the two models The rationale for proposing a pragmatic trial is to test whether tailored patient-provider communication works in real life This design allows for a large spectrum of everyday clinical settings in order to maximize applicability and generalizability The pragmatic approaches are especially pronounced along the inclusive eligibility criteria experimental intervention flexibility and primary outcome being highly relevant to patients and providers alike
The investigators will recruit from approximately 32310 adult patients from target populations southern California to enroll 134 participants in the study In addition to recruiting from the general population the investigators will place a specific emphasis on recruiting patients living in rural and underserved communities the investigators will also recruit from a full range of dermatological diseases
Patient recruitment and enrollment will begin the first month of year one and continue through the fourth month of year one The expected duration of this pragmatic single-blinded randomized controlled equivalency trial for each participant will be a maximum of 3 months including an initial baseline visit No additional follow-up visits beyond this are expected for this research study
Patients will be randomized to receive patient education via tailored or non-tailored patient-provider communication The study team will know which form of communication each patient will receive while study participants will not know the different types of communication being studied Patients randomized to either study population groups can be assessed remotely or in-person at the screeningbaseline visit At month 3 all patients will take high-quality photographs of their skin and submit these pictures to our dermatologist online Any additional in-person or remote visits will be determined by providers and patients just as they would occur in the real-world Primary and secondary outcomes will be monitored at months 0 15 and 3
The investigators will recruit from approximately 32310 adult patients from target populations southern California to enroll 134 participants in the study In addition to recruiting from the general population the investigators will place a specific emphasis on recruiting patients living in rural and underserved communities the investigators will also recruit from a full range of dermatological diseases
Patient recruitment and enrollment will begin the first month of year one and continue through the fourth month of year one The expected duration of this pragmatic single-blinded randomized controlled equivalency trial for each participant will be a maximum of 3 months including an initial baseline visit No additional follow-up visits beyond this are expected for this research study
Patients will be randomized to receive patient education via tailored or non-tailored patient-provider communication The study team will know which form of communication each patient will receive while study participants will not know the different types of communication being studied Patients randomized to either study population groups can be assessed remotely or in-person at the screeningbaseline visit At month 3 all patients will take high-quality photographs of their skin and submit these pictures to our dermatologist online Any additional in-person or remote visits will be determined by providers and patients just as they would occur in the real-world Primary and secondary outcomes will be monitored at months 0 15 and 3
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None