Actively Recruiting
The Effect of Antihypertensive Medication Use on Fall Risk: A Randomized Controlled Trial
Led by Abant Izzet Baysal University · Updated on 2026-02-12
186
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to compare the short-term effects of three commonly prescribed blood pressure medications—beta-blockers, ACE inhibitors, and calcium channel blockers—on balance and the risk of falling. The study focuses on adults aged 18 to 75 years who are newly diagnosed with primary hypertension and have not used these medications before. It addresses important questions about how these drugs may affect balance, dizziness, and fear of falling during the initial treatment period. Participants will be randomly assigned to one of three treatment groups receiving either metoprolol (a beta-blocker), ramipril (an ACE inhibitor), or amlodipine (a calcium channel blocker). The exact dosage and agent will be determined by a cardiology clinic following standard guidelines. The treatments will be given over four weeks, with evaluations at the start (baseline), two weeks, and four weeks later. During the study, participants will undergo balance testing using the Biodex Balance System, including fall risk and postural stability tests, as well as the Clinical Test of Sensory Interaction on Balance. They will also complete questionnaires measuring dizziness impact and fear of falling. These assessments will help researchers understand how the medications influence balance and fall risk. The main outcome is the fall risk score measured at three time points. The study will monitor participants for four weeks after starting treatment to collect all data.
CONDITIONS
Brief Title
Short-Term Effects of Antihypertensive Drugs on Postural Balance and Fall Risk
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged between 18 and 75 years
- Newly diagnosed with primary hypertension
- No prior use of antihypertensive medication
- No history of neurological, vestibular, orthopedic, or psychiatric conditions affecting balance
- Able to walk independently without assistive devices
- Provided written informed consent to participate in the study
You will not qualify if you...
- Secondary hypertension
- Known diagnosis of vestibular disorders (e.g., BPPV, Ménière's disease)
- Use of medications that may affect balance (e.g., sedatives, psychotropic drugs)
- History of falls due to trauma unrelated to balance
- Cognitive impairment preventing proper test participation
- Inability to complete the assessments at follow-up timepoints (2nd and 4th week)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 4 weeks
Participants receive one of three antihypertensive drug classes and undergo postural balance and fall risk assessments.
3 visits (baseline, week 2, and week 4; in-person)
Trial Site Locations
Total: 1 location
1
Bolu Abant Izzet Baysal University, Izzet Baysal Training and Research Hospital
Bolu, Turkey (Türkiye), 14030
Actively Recruiting
Research Team
A
Alp Ozel, PT, PhD
U
Umut A Ugras, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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