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Clinical Trial Summary

The aim of this study is to evaluate the feasibility and acceptability of the model of delivering CHW-driven home-based comprehensive NCD control services aimed to prevent premature deaths from cardio-vascular diseases, stroke and breast, cervix and oral cancers in the hard-to-reach women.


Clinical Trial Description

Specific objectives of this study are the evaluation of: 1. The social, cultural and behavioral factors that impact the uptake of the NCD control services among rural women using the Rapid Assessment, Response and Evaluation (RARE) approach; 2. The feasibility and acceptability of the strategy to deliver the following NCD control services to the rural women at their homes by the trained CHWs: - Counselling of the tobacco habitués to give up the practice - Early detection of hypertension and diabetes to ensure prompt and regular treatment - Creating breast awareness and ensuring access to prompt diagnosis and treatment of the women with symptoms suggestive of breast cancer - Screening for cervical cancer by self-collected HPV test and ensuring prompt treatment of screen detected precancers and cancers - Screening of the habitual tobacco/alcohol users for oral cancer by OVE and ensuring prompt treatment of screen detected precancers and cancers ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03604939
Study type Interventional
Source International Agency for Research on Cancer
Contact
Status Completed
Phase N/A
Start date January 1, 2017
Completion date July 1, 2019

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