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Isometric Exercise for Hypertension

Not Applicable
Recruiting
Conditions
Hypertension
Interventions
Behavioral: wall squat
Behavioral: passive stretching
Registration Number
NCT06515054
Lead Sponsor
Chinese University of Hong Kong
Brief Summary

Background: Isometric resistance exercises (IREs) have great potential to improve blood pressure (BP) control.

Methods: This is a pilot randomized controlled trial that will involve 50 patients with hypertension (HT) who do not meet the current physical activity guidelines defined by the World Health Organization. Participants will be randomly assigned in a 1:1 ratio using stratified and blocked randomization to either the IRE (wall squat) group or stretching exercise (active control) group. A well-structured, widely accepted, and validated 24-week wall squat program (2 minutes per exercise, 2 minutes of rest between sets, and 3 sessions per week) will be implemented, as it has been commonly used in previous research. All patients will be followed up for 24 weeks. Control group will receive exact same treatment except that IRE is replaced by frequency-matched and time-matched stretching exercise. The primary outcome measure will be rate of recruitment. Secondary outcomes will include BP parameters from 24-hour ambulatory BP monitoring

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
50
Inclusion Criteria
  • a suboptimal daytime SBP of >135-160 mmHg on a 24-h ABPM
  • reported no regular physical activity or less than that recommended for adults by the World Health Organization (e.g. <150 minutes of moderate-intensity aerobic exercise per week);
  • on stable doses of anti-HT medication(s) for ≥4 weeks if the patient is receiving drug treatments
  • agree for no drug changes during the intervention period (24 weeks);
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Exclusion Criteria
  • cannot provide informed consent
  • unwillingness to repeat ABPM
  • relative contraindications to ABPM (i.e. diagnosed atrial fibrillation, nighttime workers, occupational drivers, or patients with bleeding tendencies)
  • severe osteoarthritis pending knee replacement surgery
  • known secondary HT
  • use of ≥3 anti-HT medications at maximum doses or ≥4 anti-HT medications
  • SBP or DBP are >160 mmHg or >100 mmHg, respectively, on ABPM
  • pregnancy/breastfeeding
  • active malignancy
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
isometric exercisewall squatwall squat exercise. Each exercise session will contain 4 sets of 2-minute wall squat isometric holds with 2 minutes of rest between each set (approximately 14 minutes per session in total), and a total of 3 sessions will be arranged every week (with ideally 48 h between exercises)
passive stretchingpassive stretchingA frequency-matched (3x/week) and time-matched (\~14 minutes each session) passive static stretching exercise will be used
Primary Outcome Measures
NameTimeMethod
rate of recruitmentthrough study completion, an average of 1 year

number of people recruited per month

Secondary Outcome Measures
NameTimeMethod
Blood pressure parameters24-week after recruitment

24-hour, daytime and nighttime blood pressure from 24-hour ambulatory systolic and diastolic blood pressure measurement

flow-mediated velocity (FMD)24-week after recruitment

FMD will be performed using a high-resolution linear artery transducer couple with a software (FMD suite, Quipu, Italy) that automatically detect and measure the brachial artery diameter and will be performed according to international guidelines

Carotid-femoral pulse wave velocity24-week after recruitment

analysed by applanation tonometry using SphygmoCor (AtCor Medical Pty Ltd) with the accompanying SphygmoCor Software Suite (SphygmoCor System)

Trial Locations

Locations (1)

School of public health and primary care

🇭🇰

Hong Kong, Hong Kong

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