Smart-CKD/BP Study
Through Remote Management and Propaganda of Intelligent Mobile Phone, the Standard Rate of Blood Pressure Control and the Change of Renal Function Were Observed
1 other identifier
interventional
2
1 country
1
Brief Summary
Through remote management and propaganda of intelligent mobile phone, the standard rate of blood pressure control and the change of renal function were observed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2018
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 30, 2018
CompletedFirst Posted
Study publicly available on registry
April 18, 2018
CompletedStudy Start
First participant enrolled
May 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2019
CompletedApril 18, 2018
March 1, 2018
6 months
March 30, 2018
April 17, 2018
Conditions
Outcome Measures
Primary Outcomes (2)
Control rate of blood pressure control
Average blood pressure of each patient ,thenStatistics of the number of blood pressure control standards .
1 year
Drug compliance
Take medications according to the doctor's advice
1 year
Study Arms (2)
Management Group
OTHERcontrol group
OTHERInterventions
Through remote management and propaganda of intelligent mobile phone, the standard rate of blood pressure control and the change of renal function were observed.
Eligibility Criteria
You may qualify if:
- diagnosis in line with the 2012 international kidney disease: improving global outcomes (kidney disease improving global out-comes, KDIGO) of chronic kidney disease diagnosis standard of hypertension diagnosis, "China Hypertension Prevention Guide 2010" diagnostic criteria;
- and will have the use of intelligent mobile phone, and a network connection;
- at the age of 18-70.
You may not qualify if:
- GFR\<15 ml/min or start replacement therapy;
- do not understand Chinese, do not understand Chinese;
- malignant tumor patients;
- have mental illness;
- there is consciousness disorder.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pengli Luo
Qinghai, Xining, China
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Deputy chief physician
Study Record Dates
First Submitted
March 30, 2018
First Posted
April 18, 2018
Study Start
May 1, 2018
Primary Completion
November 1, 2018
Study Completion
May 1, 2019
Last Updated
April 18, 2018
Record last verified: 2018-03