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Community screening of participants across community pharmacies detecting asymptomatic clinical markers or risk factors associated with cardiovascular disease and chronic disease.

Early detection and management of cardiovascular risk factors and chronic disease markers in community pharmacy trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619000405112
Acronym
PTP Trial
Enrollment
200
Registered
2019-03-13
Start date
2019-09-20
Completion date
2020-06-30
Last updated
2020-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This trial will assess the clinical and cost effectiveness of two in pharmacy screening interventions to detect and enable early intervention with regards to Cardiovascular disease and prevent its complications or detect existing and related disease (eg type 2 diabetes).

Interventions

A Comprehensive risk assessment will be performed by a trained pharmacist in the community pharmacy setting. Collection of your age, gender, smoking status, blood pressure measurement and heart rate and questions from the Australian type 2 diabetes risk assessment tool (AUSDRISK) be taken. A waist measurement and a finger prick blood test that measures blood sugar and cholesterol. The Complete time of this test would be 20-30 minutes.. Blood pressure measurement and heart rate will be measure

A Comprehensive risk assessment will be performed by a trained pharmacist in the community pharmacy setting. Collection of your age, gender, smoking status, blood pressure measurement and heart rate and questions from the Australian type 2 diabetes risk assessment tool (AUSDRISK) be taken. A waist measurement and a finger prick blood test that measures blood sugar and cholesterol. The Complete time of this test would be 20-30 minutes.. Blood pressure measurement and heart rate will be measured using an omron BP machine and the finger prick blood sample will be analysed through the cobas machine with an immediate result printed. There will be the requirement to complete some validate questionnaires as part of this visit, (Ausrisk, 36 item health survey questionnaire, Health care utilisation questionnaire). Face to face contact at the pharmacy site (with a trained pharmacist performing the assessment/visit) will be required at baseline, 6 month visit and 12 month vist. A total of 3 visits for the duration of 12 month long trial will be required for consented participants. On site monitoring and source verification checks will be performed on case report forms during the 12 month trial. SMS reminders will be sent to consented participants to advise when their 6 month or 12 month visit is due. A internal database will monitor participant visit schedules to check for adherence to the protocol and documentation of any minor deviations from this for example on holiday or missed visits.

Sponsors

Blackswan Health
Lead SponsorOther

Study design

Allocation
Randomised controlled trial
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
35 Years to 74 Years
Healthy volunteers
Yes

Inclusion criteria

individuals 45-74 years individuals 35-74 years if Aboriginal or Torres strait Islander Who are able to make independent decisions regarding their health care Both Males and Females Healthy volunteers

Exclusion criteria

Diagnosed cardiovascular disease or diabetes Currently being treated for hypertension or lipid disorders Currently engaged in any lifestyle modification program

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026