Effects of Isometric Wall Squat Training on Blood Pressure in Adults With Hypertension

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19+
SponsorKorea University Guro Hospital

About this trial

This randomized controlled trial aims to evaluate whether 12 weeks of isometric wall squat (IWS) exercise can improve blood pressure control and blood pressure variability in adults with essential hypertension. Blood pressure changes during daily activities and sleep will be assessed using a ring-type continuous blood pressure monitoring device (CART BP). The primary outcome is the change in 24-hour mean systolic blood pressure after 12 weeks compared with standard hypertension care.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult men and women aged 19 years or older

Patients diagnosed with essential hypertension and undergoing outpatient follow-up

Subjects whose antihypertensive medication has been stably maintained for at least 4 weeks prior to enrollment

Clinic blood pressure of systolic blood pressure (SBP) ≥130 mmHg or diastolic blood pressure (DBP) ≥80 mmHg.

Disqualifiers

Participants with unstable angina or a diagnosis of myocardial infarction or stroke within the past 6 months.

Participants diagnosed with New York Heart Association (NYHA) functional class III-IV heart failure, severe valvular heart disease, or severe arrhythmia.

Participants with severe knee, hip, or spinal disorders that prevent them from performing wall squats.

Participants with severe renal or hepatic disease or severe cognitive impairment.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Isometric Wall Squat (IWS) Exercise

    Behavioral

    Participants perform home-based isometric wall squat (IWS) exercise three times per week for 12 weeks. Each session consists of four sets of up to 2 minutes, with 2-minute rest periods between sets. The target knee angle is individualized based on the baseline incremental IWS test. Heart rate and rating of perceived exertion are monitored during exercise.

  • Standard Hypertension Care

    Other intervention

    Participants receive standard hypertension care, including their current antihypertensive medication and lifestyle education based on hypertension guidelines. No structured isometric exercise program is provided during the intervention period.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Isometric Wall Squat Training GroupExperimental treatment 1 intervention
Group B: Standard Care GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in 24-hour mean systolic blood pressure

Change in 24-hour mean systolic blood pressure measured using a ring-type continuous blood pressure monitoring device (CART BP).

Time frame
Baseline to 12 weeks
2

Change in 24-hour mean diastolic blood pressure

Change in 24-hour mean diastolic blood pressure measured using a ring-type continuous blood pressure monitoring device (CART BP).

Time frame
Baseline to 12 weeks
3

Change in office systolic blood pressure

Change in office systolic blood pressure to evaluate ambulatory versus office blood pressure reduction.

Time frame
Baseline to 12 weeks
4

Change in office diastolic blood pressure

Change in office diastolic blood pressure to evaluate ambulatory versus office blood pressure reduction.

Time frame
Baseline to 12 weeks

Secondary outcomes

1

Change in mean daytime systolic blood pressure

Change in mean daytime systolic blood pressure measured using CART BP.

Time frame
Baseline to 12 weeks
2

Change in mean daytime diastolic blood pressure

Change in mean daytime diastolic blood pressure measured using CART BP.

Time frame
Baseline to 12 weeks
3

Change in mean nighttime systolic blood pressure

Change in mean nighttime systolic blood pressure measured using CART BP.

Time frame
Baseline to 12 weeks
4

Change in mean nighttime diastolic blood pressure

Change in mean nighttime diastolic blood pressure measured using CART BP.

Time frame
Baseline to 12 weeks

Other outcomes

Sponsors and contacts

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