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NCT07017153Completed

Patient Decision Aids for Hypertension: A Pilot Study

Evaluation of the Impact of Decision Aids on Treatment Choices in Patients With Arterial Hypertension: A Pilot Study

Source: ClinicalTrials.gov · Last updated 12 Jun 2025

Brief summary (registry, in English)

Background: Arterial hypertension is a major global health problem with a leading cause of premature death and a major risk factor for cardiovascular disease. Despite its prevalence, blood pressure control remains suboptimal, requiring effective treatment and patient engagement strategies. With the increasing emphasis on person-centered care, healthcare professionals and patients are moving toward shared decision-making (SDM), which is defined as an approach to collaboratively making health decisions in line with recent evidence and patient preferences and values. Patient decision aids (PDAs) are tools designed to involve patients in treatment decisions by providing clear information about options, benefits and risks, while helping them to clarify personal values. These tools have been shown to improve decision quality, adherence and health outcomes. Methods: This pilot study aims to evaluate the practical utility of two PDAs with different formats for antihypertensive therapy from the patient's perspective. Adult patients (≥ 18 years) with hypertension admitted to a university hospital will be randomized to use one of the two PDAs displayed on a tablet. After viewing the PDA, participants will complete a questionnaire assessing their knowledge, risk perception, preferences, and involvement in decision-making. Descriptive statistics will be used to analyze the data. Expected results: The study anticipates that the PDAs will increase patients knowledge of treatment options, support value clarification and improve engagement in SDM. These findings will inform the design of a larger randomized controlled trial to optimize PDA formats for hypertension management.

Status (registry)
Completed
Study type
Interventional
Enrollment
60 (actual)
First submitted
16 Apr 2025
Start date
27 Feb 2025
Primary completion date
15 Apr 2025
Lead sponsor
Medizinische Hochschule Brandenburg Theodor Fontane
NCT number
NCT07017153

What you commit to

  • Study type: Interventional
  • Participants enrolled: 60
  • From 27 Feb 2025 to the primary completion date, 15 Apr 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Pregnancy-induced hypertension

Age

  • Patients under 18 years old

Other

  • Patients unable to provide informed consent

Who the study is looking for

  • Adults (\>18 years)
  • Diagnosed with hypertension (all stages), regardless of primary reason for treatment.
  • Receiving treatment at the Department of Internal Medicine I, University Hospital Brandenburg an der Havel

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Universitätsklinikum Brandenburg an der Havel, Hochstraße 29, 14770 Brandenburg an der Havel
Coordinator of this site? Confirm its status
Brandenburg an der HavelGermanyUnknown status
Institute for Health Services and Health System Research, Faculty of Health Science Brandenburg, Brandenburg Medical School (Theodor Fontane)
Coordinator of this site? Confirm its status
RüdersdorfGermanyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.