- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04418947
Project Resurgence Communication Trial
October 26, 2021 updated by: Anne Cappola, MD, University of Pennsylvania
Comparison of the Effectiveness of Communication Strategies on the Return to In-Person Visits to a Medical Center After the Emergence of COVID-19: A Randomized Trial
Randomized, double-blind, of standard of care vs additional communication and factorial design of intervention letter vs. control letter and EHR vs mail delivery mechanism in patients who canceled visits and did not reschedule over a 90 day period starting March 9, 2020.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
11120
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19104
- University of Pennsylvania
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients with a cancellation or failure to show for a procedure or visit from March 9, 2020 through June 7, 2020 (90 days) and who have not rescheduled as of the date of randomization
Exclusion Criteria:
- Death
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: No intervention
|
|
Active Comparator: MPM control letter
|
Control letter vs. intervention letter
|
Experimental: MPM intervention letter
|
Control letter vs. intervention letter
|
Active Comparator: Mailed control letter
|
Control letter vs. intervention letter
|
Experimental: Mailed intervention letter
|
Control letter vs. intervention letter
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Percent of Participants With Visit or Procedure With Provider
Time Frame: 1 month
|
1 month
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Percent of Participants With Scheduled Visit or Procedure With Provider
Time Frame: 1 month
|
1 month
|
Percent of Participants With Completed Telemedicine Visit With Provider
Time Frame: 1 month
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 15, 2020
Primary Completion (Actual)
July 17, 2020
Study Completion (Actual)
July 17, 2020
Study Registration Dates
First Submitted
May 29, 2020
First Submitted That Met QC Criteria
June 2, 2020
First Posted (Actual)
June 5, 2020
Study Record Updates
Last Update Posted (Actual)
October 28, 2021
Last Update Submitted That Met QC Criteria
October 26, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 843220
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Communication Research
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Insel Gruppe AG, University Hospital BernSwiss National Science Foundation; University of Bern; Fachhochschule NordwestschweizRecruitingCommunication Research | Communication, MultidisciplinarySwitzerland
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University of MinnesotaNational Cancer Institute (NCI)CompletedCommunication ResearchUnited States
-
University of Wisconsin, MadisonRecruitingCommunication ResearchUnited States
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Duke-NUS Graduate Medical SchoolCompletedCommunication ResearchSingapore
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Abramson Cancer Center at Penn MedicineUniversity of FloridaRecruitingCommunication Research | Adolescent Behavior | VapingUnited States
-
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-
State University of New York at BuffaloCompletedCommunication ResearchUnited States
-
University of FloridaEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompletedCommunication Research | Attitude of Health Personnel | Trust | Attitude to Computers | Researcher-Subject RelationsUnited States
Clinical Trials on Communication type
-
Swansea UniversityCompletedControl Condition | Positive Communication (Primary) | Negative CommunicationUnited Kingdom
-
University of OxfordNIHR Collaboration for Leadership in Applied Health Research and Care (Oxford)CompletedType 2 Diabetes MellitusUnited Kingdom
-
University of RochesterNational Institutes of Health (NIH)Not yet recruiting
-
Hugo W. Moser Research Institute at Kennedy Krieger...HRSA/Maternal and Child Health BureauCompleted
-
University of Southern CaliforniaUniversity of PittsburghRecruitingHypertensionUnited States
-
HAN University of Applied SciencesNot yet recruitingChronic Pain | CommunicationNetherlands
-
HAN University of Applied SciencesCompleted
-
Riphah International UniversityCompleted
-
University of MichiganNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Enrolling by invitationFocal Segmental Glomerulosclerosis | Minimal Change Disease | Membranous Nephropathy | Nephrotic Syndrome in Children | FSGS | MCD | Minimal Change Nephrotic Syndrome | MCD - Minimal Change DiseaseUnited States
-
Montefiore Medical CenterRecruitingCritical Illness | Terminal IllnessUnited States