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Implementation of a mobile technology supported cardiovascular disease prevention program in Indonesia and North India.

Not Applicable
Completed
Registration Number
CTRI/2017/08/009387
Lead Sponsor
George Institute for Global Health Australia
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
584
Inclusion Criteria

participants between 40-85 years

Exclusion Criteria

Respondents where measurements for blood pressure, height and weight not possible i.e. incapacitated respondents

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Indonesia: Difference in the change in the proportion from baseline to end-of-study of high risk individuals prescribed appropriate preventive medications between the intervention and control arms. <br/ ><br> <br/ ><br>India: Difference in the proportion of high risk individuals prescribed appropriate preventive medications between the screening phase (identified by ASHA) and end of the study evaluation (among those identified as high risk by ASHA during screening)Timepoint: By February 2018
Secondary Outcome Measures
NameTimeMethod
Indonesia: Diff in the change in the proportion from baseline to end-of-study (EOS) of high risk individuals (HRI) achieving SBP less than 140mmHg between the int and cont arms. <br/ ><br>Diff in mean reduction in BP levels between the int and cont arms. <br/ ><br>% of HRI correctly referred and followed-up by NPHWs in the intervention arm. <br/ ><br> <br/ ><br>India: % HRI correctly referred by NPHWs to PHC doctors <br/ ><br>% HRI receiving follow-up visits by NPHWs <br/ ><br>% HRI achieving blood pressure targetsTimepoint: By February 2018
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