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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02388542
Other study ID # PROGRESS-IND-1022015
Secondary ID
Status Active, not recruiting
Phase N/A
First received February 9, 2015
Last updated September 13, 2017
Start date May 2015
Est. completion date December 2017

Study information

Verified date October 2016
Source St. John's Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators propose conducting a pilot study to identify 6 worksites (2 India, 2 Sri Lanka, 2 Bangladesh) explore barriers to optimum cardiovascular disease(CVD) care at these worksites, quantify risk factor level in worksite populations and identify and train peer mentors to deliver an educational intervention to improve life style and enhance medication adherence among those at moderate to high risk of cardiovascular disease (CVD).


Description:

Eligibility Criteria -

All employees aged above 35 years at selected workplaces.

Study design - Mixed methods methods Phase 1 - Qualitative study; Phase 2 - Quantitative - Single group, non-randomized before-after comparison study + KAP survey

Sample size - Approximately 334 participants.

The study entails the following steps -

Step 1 - An evaluation for knowledge, attitudes and practices (KAP) related to cardiovascular health/ disease at worksites.

Step 2 - A qualitative study for barriers and facilitators of behaviors associated with optimal cardiovascular health

Step 3 - Baseline assessment of cardiovascular risk using a non-lab based risk assessment score

Step 4 - Piloting a trained peer mentored educational/ intensive follow-up intervention for 3 month with a re-assessment at 3 months.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 334
Est. completion date December 2017
Est. primary completion date October 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 35 Years to 70 Years
Eligibility Inclusion Criteria:

- All criteria must be met to be eligible

1. Employees (Men & Women) above the age of 35 years.

2. permanent employees with at least 6 months for retirement.

3. Willing to provide Informed Consent.

Exclusion Criteria:

- Subject ineligible if even one criterion is met

1. Pregnant or intent to get pregnant in one year.

2. Inability to attend follow up visits.

3. Any active malignancy or known malignancy on treatment.

4. Will relocate during the study period.

5. Unwilling or unable to comply with study procedures.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Educational Intervention
Employees above the age of 35 years will be risk stratified into moderate or high risk of developing cardiovascular disease using a simple non-lab based risk scoring system, they will be invited to participate in the pilot intervention study. This is a single arm before-after study.subject education will focus on life style medication and adherence to medication (if applicable).importantly the peer mentor will try to identify barriers to adopting a healthy lifestyle(tobacco, physical acitivity, diet, alcohol and strees) and adherence to cardiovascular disease prevention medication. peer mentors will be trained to interpret blood glucose and lipids, recognize abnormal valves, provide lifestyle counseling and refer to treating physician when appropriate.

Locations

Country Name City State
Bangladesh Appollo Ispat Complex Ltd Dhaka
Bangladesh Shardharan Bima Coorporation Dhaka
India Bharat Heavy Electrical Limited Bangalore
India TVS Motor company Limited Hosur
Sri Lanka Department of Census & Statistics Colombo
Sri Lanka Sri Lanka Telecom Colombo

Sponsors (4)

Lead Sponsor Collaborator
St. John's Research Institute International Centre for Diarrhoeal Disease Research, Bangladesh, University of Colombo, University of Oxford

Countries where clinical trial is conducted

Bangladesh,  India,  Sri Lanka, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in knowledge attitudes & practices related to Cardiovascular risk factors. (questionnaire) A knowledge, attitudes & practices questionnaire will be administered to participants 1 Month
Primary Identification of barriers and facilitators for an optimal Cardiovascular Health environment. (In depth interviews and focus groups discussions with random sample of participants) qualitative analysis - In depth interviews and focus groups discussions with random sample of participants 3 Months
Primary Estimate the Cardiovascular risk factor burden (validated non lab based Cardiovascular risk score) validated non lab based Cardiovascular risk score will be used (developed from NHANES data and validated against Framingham score 3 Months
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