- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04731194
Promoting Medication Reimbursement Policy (PAPMed) (PAPMed)
July 17, 2021 updated by: Duke Kunshan University
Promoting the Adoption of Local Government Policy on the Reimbursement of Chronic Disease Medicines (PAPMed): a Field-based Cluster-Randomized Controlled Trial in Rural Nantong, China
Rationale: Chronic non-communicable diseases (NCDs) have become the leading cause of morbidity and mortality in China.
Rural NCDs patients are more likely to suffer from poverty.
Nantong city has established a reimbursement plan covering 50% of hypertension and diabetes medication costs, however, various barriers prevent patients from taking advantage of this policy.
Objectives: To evaluate the effectiveness of the intervention on saving medical costs and promoting health in rural populations.
Study design: a cluster-randomized controlled trial.
Study population: village doctors and health insurance officials at township hospitals are implementors of the intervention.
Patients in the basic public health service system are the target populations of the intervention.
Randomization: 31 villages are included in the study. 1 village is randomly dropped, and the rest of the villages will be randomly assigned to the intervention and control group stratified by township with an allocation ratio of 1:1.
Intervention and follow-up: village doctors will promote policy awareness and support patients registration.
They will follow-up patients on the 1st, 3rd, and 6th month and receive financial incentives based on their performance of supporting patients registration and encouraging patients to buy medications in designated medical institutions to be reimbursed.
Control: The control group would serve as a natural baseline and do not receive any intervention.
Outcomes: Patients' registration rate, medical costs saved, medication compliance rate, and improvements on health indicators will be evaluated based on real-world medical examination, prescription, and insurance data.
Sample size: an estimated sample of 5000 patients from 30 clusters will be registered in the policy.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Rationale: Chronic non-communicable diseases (NCDs) have become the leading cause of morbidity and mortality in China.
Rural NCDs patients are more likely to suffer from poverty.
Nantong city has established a reimbursement plan covering 50% of hypertension and diabetes medication costs, however, various barriers prevent patients from taking advantage of this policy.
Objectives: To evaluate the effectiveness of the intervention on saving medical costs and promoting health in rural populations.
Study design: a cluster-randomized controlled trial.
Study population: village doctors and health insurance officials at township hospitals are implementors of the intervention.
Patients in the basic public health service system are the target populations of the intervention.
Randomization: 31 villages are included in the study. 1 village is randomly dropped, and the rest of the villages will be randomly assigned to the intervention and control group stratified by township with an allocation ratio of 1:1.
Intervention and follow-up: village doctors will promote policy awareness and support patients registration.
They will follow-up patients on the 1st, 3rd, and 6th month and receive financial incentives based on their performance of supporting patients registration and encouraging patients to buy medications in designated medical institutions to be reimbursed.
Control: The control group would serve as a natural baseline and do not receive any intervention.
Outcomes: Patients' registration rate, medical costs saved, medication compliance rate, and improvements on health indicators will be evaluated based on real-world medical examination, prescription, and insurance data.
Sample size: an estimated sample of 5000 patients from 30 clusters will be registered in the policy.
Study Type
Interventional
Enrollment (Anticipated)
5000
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 Contact
- Name: Lijing Yan
- Phone Number: (+86) 512 3665 7057
- Email: lijing.yan@duke.edu
Study Contact Backup
- Name: Yuexia Gao
- Phone Number: 13962968819
- Email: 386912453@qq.com
Study Locations
-
-
Jiangsu
-
Nantong, Jiangsu, China, 226019
- Recruiting
- Nantong University
-
Contact:
- Yuexia Gao
- Phone Number: 13962968819
- Email: 386912453@qq.com
-
-
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
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion criteria:
To be eligible to register in the medication reimbursement policy, patients need to be:
- Living in the service areas of the village clinics
- Officially diagnosed with hypertension and/or diabetes in a township level hospital or above
- Registered as a hypertensive and/or diabetic patient in the public health service system
Exclusion criteria:
Not part of the New Cooperative Medical Scheme (NCMS) for rural residents
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: HEALTH_SERVICES_RESEARCH
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: performance-based financial incentive program
Village doctors in villages of the intervention group will promote policy awareness, support registration, follow-up patients, and receive financial incentives based on their performance.
|
|
|
NO_INTERVENTION: current situation
Village doctors in villages of the control group will not be contacted.
The control group would serve as a natural baseline and do not receive any intervention.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Registration Rate
Time Frame: 6 months
|
The percentage of patients registered to the policy in the health insurance system
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Registration number
Time Frame: 6 months
|
The number of all registered patients in the village served by the village clinic
|
6 months
|
|
Medical costs saved
Time Frame: 6 months
|
The amount of money saved on outpatient expenses, hospital expenses, personal out-of-pocket expenses, and medical insurance reimbursement expenses
|
6 months
|
|
Doctor visiting frequency
Time Frame: 6 months
|
Rate and visiting frequency of registered patients seeing doctors in designated hospitals
|
6 months
|
|
Medication compliance rate
Time Frame: 6 months
|
Prescription frequency and doses, medication purchasing rate among registered patients, times of reimbursement during intervention and follow-up period among registered patients, insulin usage rate among registered diabetic patients
|
6 months
|
|
Blood pressure
Time Frame: 6 months
|
Average systolic and diastolic blood pressure level among all rural hypertensive patients
|
6 months
|
|
Blood glucose
Time Frame: 6 months
|
Average blood glucose level among rural diabetic patients
|
6 months
|
|
Blood lipids
Time Frame: 6 months
|
Average blood lipids level among rural hypertensive and diabetic patients
|
6 months
|
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)
January 30, 2021
Primary Completion (ANTICIPATED)
August 31, 2021
Study Completion (ANTICIPATED)
October 30, 2021
Study Registration Dates
First Submitted
January 14, 2021
First Submitted That Met QC Criteria
January 28, 2021
First Posted (ACTUAL)
January 29, 2021
Study Record Updates
Last Update Posted (ACTUAL)
July 20, 2021
Last Update Submitted That Met QC Criteria
July 17, 2021
Last Verified
July 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020DUKE0002
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.
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