Hypertension Clinical Trial
Official title:
Hypertension Management in Young Adults Personalised by Echocardiography and Clinical Outcome.
HyperEcho is a multi-centre longitudinal observational study, to investigate whether baseline transthoracic echocardiography along with routine data collected in the hypertension clinic can guide clinicians to better manage, and improve risk stratification for cardiovascular disease in young adults with hypertension. Participants are characterised as young adult patients aged between 18 to 40 years old and referred to the hypertension clinic to manage their blood pressure. The study visit will be carried out during the planned routine visit of the participants to the hypertension clinics of NHS trusts within England. Routine data will be collected by the assigned nurse for the hypertension clinic as part of the clinical service, and research participation will not affect the clinical progress of the participant. The additional research component to the clinic will be asking the participants for their consent to undergo a research echocardiography scan if it has not been a part of their clinical assessment. Participants will also be asked to consent to the use of their data that has been collected in the hypertension clinic, such as; referral letters, medical history, 24-hour blood pressure monitoring report, ECG, blood samples, body fat composition, and dietary questionnaire. In addition to this, participants will be asked to consent to further review of their data and medical notes during their follow up visits (up to 10 years).
HyperEcho is a multi-centre longitudinal observational study, to investigate whether baseline
transthoracic echocardiography along with routine data collected in the hypertension clinic
can guide clinicians to better manage, and improve risk stratification for cardiovascular
disease in young adults with hypertension. Participants are characterised as hypertensive
patients aged between 18 to 40 years old and referred to the hypertension clinic to manage
their blood pressure. A patient and public involvement exercise has been performed to ensure
this study design would appeal to patients attending the hypertension clinic, and to
investigate the preferred method of contact.
The study visit will be carried out during the planned routine visit of the participants to
the hypertension clinics of NHS trusts within England. Routine data will be collected by the
assigned nurse for the hypertension clinic as part of the clinical service, and research
participation will not affect the clinical progress of the participant. The additional
research component to the clinic will be asking the participants for their consent to undergo
a research echocardiography scan if it has not been a part of their clinical assessment.
Participants will also be asked to consent to the use of their data that has been collected
in the hypertension clinic, such as; referral letters, medical history, 24-hour blood
pressure monitoring report, ECG, blood samples, body fat composition, and dietary
questionnaire. In addition to this, participants will be asked to consent to further review
of their data and medical notes during their follow up visits (up to 10 years).
Previous young adult patients who visited the Hypertension clinics in the last 10 years will
be also recruited. This cohort will be asked to consent to allow the research team to collect
and use their clinical data as well as follow up their medical notes. They will not actively
participate in the study as they will not require visiting the hypertension clinic or
undergoing an echocardiography scan.
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