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Clinical Trials/CTRI/2019/04/018861
CTRI/2019/04/018861Not yet recruitingNot Applicable

IMPACT OF PHARMACEUTICAL CARE ON CLINICAL OUTCOMES AND QUALITY OF LIFE FOR CORONARY HEART DISEASE PATIENTS IN A TERTIARY CARE TEACHING HOSPITAL

Nitte University1 site in 1 country290 target enrollmentStarted: May 5, 2019Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
290
Locations
1
Primary Endpoint
improvement in blood pressure, total cholesterol, blood glucose,Body mass index,medication adherence

Study Overview

Brief Summary

It is an interventional study on impact of pharmaceutical care on clinical outcomes and quality of life for coronary heart disease patients in a tertiary care teaching hospital. Objectives of the study: 1) To study the impact on quality of life (QOL) in coronary heart disease patients who have been provided with pharmaceutical care. 2) To study the impact of pharmaceutical care service such as patient counselling, medication review, patient education on clinical outcome.3) Development, validation and readability of patient information leaflet. Study will be conducted inpatients of coronary heart disease with or without comorbidities in cardiology department of a justice kS Hegde Charitable Hospital, Deralakatte Mangalore. Data will be collected from patient case sheets, treatment charts. Quality of life and medication adherence will be assessed by using Mac-new questionnaires and Morisky green levine respectively. Pharmaceutical care services like patient counselling on diet, lifestyle modification and medication improves the clinical outcomes.

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
Not Applicable

Eligibility Criteria

Ages
18.00 Year(s) to 80.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients aged 18 years and above diagnosed with coronary heart disease with or without comorbidities.

Exclusion Criteria

  • Pregnant patients.
  • Psychiatric patients.

Outcomes

Primary Outcomes

improvement in blood pressure, total cholesterol, blood glucose,Body mass index,medication adherence

Time Frame: 6 and 12 months

Secondary Outcomes

  • Development, validation and readability of patient information leaflet.(single.)

Investigators

Sponsor Class
Other [Nitte Deemed to be University]

Study Sites (1)

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