ClinicalTrials.gg
RecruitingNCT07868822ISO-BPUpdated Oct 9, 2026

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

An interventional study of Isometric Wall Squat (IWS) Exercise and Standard Hypertension Care in Essential Hypertension, sponsored by Korea University Guro Hospital. Recruiting at 1 site in South Korea. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by Korea University Guro Hospital · Not applicable, Interventional, and Treatment

Updated Oct 9, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
19 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

This study is a single-center, randomized controlled trial evaluating the antihypertensive effects of isometric wall squat (IWS) exercise in adults with essential hypertension.

Approximately 100 participants will be randomly assigned in a 1:1 ratio to either the IWS exercise group or the control group. The IWS exercise group will perform home-based isometric wall squat exercise three times per week for 12 weeks. Each exercise session will consist of four sets of up to 2 minutes, with 2-minute rest periods between sets. Exercise intensity will be individualized based on the participant's baseline incremental IWS test.

The control group will continue standard hypertension care, including current antihypertensive medication and lifestyle education based on hypertension guidelines, without a structured isometric exercise program during the intervention period.

Blood pressure will be assessed using CART BP, a ring-type continuous blood pressure monitoring device, for 24 hours at baseline and at 12 weeks. The primary outcome is the change in 24-hour mean systolic blood pressure from baseline to 12 weeks. Secondary outcomes include 24-hour mean diastolic blood pressure, daytime and nighttime blood pressure, morning blood pressure, dipping/non-dipping pattern, blood pressure variability, office blood pressure, physical function, quality of life, exercise self-efficacy, and exercise adherence.

Participants will undergo baseline assessment, an intermediate assessment at 4-6 weeks, and a final assessment at 12 weeks. Participants who wish to continue follow-up may undergo an additional assessment approximately 6 months after completion of the intervention.

02

Conditions studied

  • Essential Hypertension

Keywords

  • Isometric Wall Squat
  • Isometric Exercise
  • Blood Pressure
  • Blood Pressure Variability
  • Continuous Blood Pressure Monitoring
  • Randomized Controlled Trial
03

In context

Essential Hypertension

538 studies on the registry are indexed under Essential Hypertension; 76 are open to participants now.

This study's planned enrollment of 100 is below the median of 166 across 458 interventional studies indexed under Essential Hypertension.

Browse Essential Hypertension studies →

Lead sponsor

Korea University Guro Hospital is the lead sponsor of 89 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Adult men and women aged 19 years or older
  2. Patients diagnosed with essential hypertension and undergoing outpatient follow-up
  3. Subjects whose antihypertensive medication has been stably maintained for at least 4 weeks prior to enrollment
  4. Clinic blood pressure of systolic blood pressure (SBP) ≥130 mmHg or diastolic blood pressure (DBP) ≥80 mmHg.
  5. Participants who are able to perform wall squats and who have provided written informed consent after receiving an explanation of the study and reviewing the informed consent form

Exclusion criteria

Exclusion Criteria:

  1. Participants with unstable angina or a diagnosis of myocardial infarction or stroke within the past 6 months.
  2. Participants diagnosed with New York Heart Association (NYHA) functional class III-IV heart failure, severe valvular heart disease, or severe arrhythmia.
  3. Participants with severe knee, hip, or spinal disorders that prevent them from performing wall squats.
  4. Participants with severe renal or hepatic disease or severe cognitive impairment.
  5. Participants who are currently pregnant or have the potential to become pregnant.
  6. Participants aged 65 years or older who have a score of 3-5 (frail) on the K-FRAIL scale. However, such participants may be allowed to participate on an individual basis, following consultation with the Principal Investigator, if the treating physician clinically determines that the intervention can be performed safely.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Isometric Wall Squat Training Group

    Participants perform a 12-week home-based isometric wall squat training program in addition to standard hypertension care.

    Behavioral: Isometric Wall Squat (IWS) Exercise

  • Active comparator
    Standard Care Group

    Participants receive standard hypertension care, including current antihypertensive medication and lifestyle education based on hypertension guidelines, without a structured isometric exercise program during the intervention period.

    Other: Standard Hypertension Care

Interventions

  • BehavioralIsometric Wall Squat (IWS) Exercise

    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.

  • OtherStandard Hypertension Care

    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.

06

What researchers measure

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

  5. Change in nocturnal systolic blood pressure dipping pattern

    Assessment of nocturnal systolic blood pressure dipping pattern (dipping vs. non-dipping).

    Time frame: Baseline to 12 weeks

  6. Change in nocturnal diastolic blood pressure dipping pattern

    Assessment of nocturnal diastolic blood pressure dipping pattern (dipping vs. non-dipping).

    Time frame: Baseline to 12 weeks

  7. Change in blood pressure variability evaluated by standard deviation

    Assessment of blood pressure variability evaluated by standard deviation (SD).

    Time frame: Baseline to 12 weeks

  8. Change in blood pressure variability evaluated by coefficient of variation

    Assessment of blood pressure variability evaluated by coefficient of variation (CV).

    Time frame: Baseline to 12 weeks

  9. Change in blood pressure variability evaluated by average real variability

    Assessment of blood pressure variability evaluated by average real variability (ARV).

    Time frame: Baseline to 12 weeks

  10. Change in 30-second chair stand test performance

    Change in the number of repetitions completed during the 30-second chair stand test.

    Time frame: Baseline to 12 weeks

  11. Change in maximal handgrip strength

    Change in maximal handgrip strength measured in kilograms (kg) using a hand dynamometer.

    Time frame: Baseline to 12 weeks

  12. Change in target knee angle maintenance time during incremental isometric wall squat test

    Change in target knee angle maintenance time (measured in seconds) during the incremental isometric wall squat (IWS) test.

    Time frame: Baseline to 12 weeks

  13. Change in heart rate response during incremental isometric wall squat test

    Change in heart rate response (measured in beats per minute) during the incremental isometric wall squat (IWS) test.

    Time frame: Baseline to 12 weeks

  14. Change in physical activity level

    Change in total physical activity measured using the Global Physical Activity Questionnaire (GPAQ).

    Time frame: Baseline to 12 weeks

  15. Change in perceived stress score

    Change in perceived stress level assessed using the Korean version of the Perceived Stress Scale-10 (K-PSS-10). Total scores range from 0 to 40, where higher scores indicate higher levels of perceived stress.

    Time frame: Baseline to 12 weeks

07

Study locations

1 of 1 sites recruiting
  • Korea University Guro Hospital
    Seoul, Seoul 08308, South Korea
    Recruiting
08

References and documents

Publications

  • Taylor KA, Wiles JD, Coleman DA, Leeson P, Sharma R, O'Driscoll JM. Neurohumoral and ambulatory haemodynamic adaptations following isometric exercise training in unmedicated hypertensive patients. J Hypertens. 2019 Apr;37(4):827-836. doi: 10.1097/HJH.0000000000001922. PubMed 30817465 ↗
  • Lea JWD, O'Driscoll JM, Wiles JD. The implementation of a home-based isometric wall squat intervention using ratings of perceived exertion to select and control exercise intensity: a pilot study in normotensive and pre-hypertensive adults. Eur J Appl Physiol. 2024 Jan;124(1):281-293. doi: 10.1007/s00421-023-05269-2. Epub 2023 Jul 17. PubMed 37458822 ↗
  • Cohen DD, Aroca-Martinez G, Carreno-Robayo J, Castaneda-Hernandez A, Herazo-Beltran Y, Camacho PA, Otero J, Martinez-Bello D, Lopez-Lopez JP, Lopez-Jaramillo P. Reductions in systolic blood pressure achieved by hypertensives with three isometric training sessions per week are maintained with a single session per week. J Clin Hypertens (Greenwich). 2023 Apr;25(4):380-387. doi: 10.1111/jch.14621. Epub 2023 Mar 25. PubMed 36965163 ↗
  • Lee H, Park S, Kwon H, Cho B, Park JH, Lee HY. Feasibility and Effectiveness of a Ring-Type Blood Pressure Measurement Device Compared With 24-Hour Ambulatory Blood Pressure Monitoring Device. Korean Circ J. 2024 Feb;54(2):93-104. doi: 10.4070/kcj.2023.0303. Epub 2023 Dec 26. PubMed 38196118 ↗
  • Wiles JD, Goldring N, Coleman D. Home-based isometric exercise training induced reductions resting blood pressure. Eur J Appl Physiol. 2017 Jan;117(1):83-93. doi: 10.1007/s00421-016-3501-0. Epub 2016 Nov 16. PubMed 27853886 ↗
  • Goldring N, Wiles JD, Coleman D. The effects of isometric wall squat exercise on heart rate and blood pressure in a normotensive population. J Sports Sci. 2014;32(2):129-36. doi: 10.1080/02640414.2013.809471. Epub 2013 Jul 24. PubMed 23879248 ↗
  • Wiles, J. D., Goldring, N., O'Driscoll, J. M., Taylor, K. A., & Coleman, D. A. (2018). An alternative approach to isometric exercise training prescription for cardiovascular health. Transl J Am Coll Sports Med, 3(2), 10-8.
  • Edwards JJ, Wiles J, O'Driscoll J. Mechanisms for blood pressure reduction following isometric exercise training: a systematic review and meta-analysis. J Hypertens. 2022 Nov 1;40(11):2299-2306. doi: 10.1097/HJH.0000000000003261. Epub 2022 Aug 8. PubMed 35950976 ↗
  • Gebreyohannes EA, Bhagavathula AS, Abebe TB, Tefera YG, Abegaz TM. Adverse effects and non-adherence to antihypertensive medications in University of Gondar Comprehensive Specialized Hospital. Clin Hypertens. 2019 Jan 15;25:1. doi: 10.1186/s40885-018-0104-6. eCollection 2019. PubMed 30675379 ↗
  • Mills KT, Bundy JD, Kelly TN, Reed JE, Kearney PM, Reynolds K, Chen J, He J. Global Disparities of Hypertension Prevalence and Control: A Systematic Analysis of Population-Based Studies From 90 Countries. Circulation. 2016 Aug 9;134(6):441-50. doi: 10.1161/CIRCULATIONAHA.115.018912. PubMed 27502908 ↗
  • GBD 2019 Risk Factors Collaborators. Global burden of 87 risk factors in 204 countries and territories, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet. 2020 Oct 17;396(10258):1223-1249. doi: 10.1016/S0140-6736(20)30752-2. PubMed 33069327 ↗

Individual participant data

Plan to share: Undecided

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 9, 2026
Show all 1 update
  1. Oct 9, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07868822
Lead sponsor
Korea University Guro Hospital
Responsible party
Na, Jin Oh (Professor, Korea University Guro Hospital) — Principal investigator
First posted
Oct 9, 2026
Start date
Sep 29, 2026
Primary completion
Dec 2029 (estimated)
Completion
Dec 31, 2029 (estimated)
Last update
Oct 9, 2026

Study contacts

Jin-Oh Na, MD, PhD
Contact
koolup93@gmail.com
82-2-2626-3025 ext. 1058
Jin-Oh Na, MD, PhD
principal investigator · Korea University Guro Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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