NCT07251920

Brief Summary

High blood pressure is prevalent in a third of the global population and is a key risk factor for cardiovascular disease, the leading cause of death. one lifestyle change that is recommended to reduce blood pressure is to exercise, typically by performing aerobic exercise, but this is often not well adhered to, given the physical and time demands associated with it. Isometric resistance training has been evidenced as an efficacious method to reduce blood pressure, even when performing four two-minute contractions per day, three days per week at 30% of maximum effort. At present, the dose-response effects have not been examined, which are required to identify the minimal effective dose, which could further reduce the temporal demands of this modality to potentially enhance adhernece even more in time-anxious individuals. Therefore, this study aimed to compare the efficacy of once- twice-, and thrice-weekly isometric resistance training programmes to lower blood pressure,

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for phase_3 hypertension

Timeline
Completed

Started Feb 2024

Shorter than P25 for phase_3 hypertension

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 19, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 20, 2024

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 21, 2024

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

November 18, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

November 26, 2025

Completed
Last Updated

November 26, 2025

Status Verified

January 1, 2024

Enrollment Period

3 months

First QC Date

November 18, 2025

Last Update Submit

November 18, 2025

Conditions

Keywords

HypertensionBlood pressureIsometric contractionIsometric resistance trainingIsometric exercise

Outcome Measures

Primary Outcomes (1)

  • Ambulatory blood pressure

    Blood pressure assessed during a 24-hour window

    Through study completion (12 weeks)

Secondary Outcomes (1)

  • Resting blood pressure

    Through study completion (12 weeks)

Study Arms (3)

Once-weekly training

EXPERIMENTAL

Performed isometric resistance training once per week (four 2-minute contractions).

Other: Isometric resistance training

Twice-weekly training

EXPERIMENTAL

Performed isometric resistance training twice per week (eight 2-minute contractions).

Other: Isometric resistance training

Thrice-weekly training

ACTIVE COMPARATOR

Performed isometric resistance training thrice per week (12 2-minute contractions).

Other: Isometric resistance training

Interventions

isometric resistance training was performed on the chest, arms, and leg muscle groups using a band. Each contraction, was pulled at a perceived 30% (using a CR10 perceieved exertion rating scale) of maximum effort for 2 minutes; one repetition was performed using each muscle group. Weekly frequnecy changed between groups, ranging from once to thrice per week.

Once-weekly trainingThrice-weekly trainingTwice-weekly training

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • not taking anti-hypertensive medication
  • borderlerine hypertensive or hypertensive (systolic blood pressure \>139 mmHG, diastolic blood pressure \> 89 mmHg

You may not qualify if:

  • conditoned to resistance training
  • currently taking anti-hypertensive medication
  • regularly smoke or vape
  • are pregnant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Northampton, Waterside Campus

Northampton, Northamptonshire, NN1 5PH, United Kingdom

Location

Related Publications (4)

  • Smart NA, Way D, Carlson D, Millar P, McGowan C, Swaine I, Baross A, Howden R, Ritti-Dias R, Wiles J, Cornelissen V, Gordon B, Taylor R, Bleile B. Effects of isometric resistance training on resting blood pressure: individual participant data meta-analysis. J Hypertens. 2019 Oct;37(10):1927-1938. doi: 10.1097/HJH.0000000000002105.

    PMID: 30889048BACKGROUND
  • Lopes S, Felix G, Mesquita-Bastos J, Figueiredo D, Oliveira J, Ribeiro F. Determinants of exercise adherence and maintenance among patients with hypertension: a narrative review. Rev Cardiovasc Med. 2021 Dec 22;22(4):1271-1278. doi: 10.31083/j.rcm2204134.

    PMID: 34957769BACKGROUND
  • Zhou B, Perel P, Mensah GA, Ezzati M. Global epidemiology, health burden and effective interventions for elevated blood pressure and hypertension. Nat Rev Cardiol. 2021 Nov;18(11):785-802. doi: 10.1038/s41569-021-00559-8. Epub 2021 May 28.

    PMID: 34050340BACKGROUND
  • Garcia-Hermoso A, Lopez-Gil JF, Ramirez-Velez R, Alonso-Martinez AM, Izquierdo M, Ezzatvar Y. Adherence to aerobic and muscle-strengthening activities guidelines: a systematic review and meta-analysis of 3.3 million participants across 32 countries. Br J Sports Med. 2023 Feb;57(4):225-229. doi: 10.1136/bjsports-2022-106189. Epub 2022 Nov 23.

    PMID: 36418149BACKGROUND

MeSH Terms

Conditions

Hypertension

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular Diseases

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Parallel
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 18, 2025

First Posted

November 26, 2025

Study Start

February 19, 2024

Primary Completion

May 20, 2024

Study Completion

May 21, 2024

Last Updated

November 26, 2025

Record last verified: 2024-01

Data Sharing

IPD Sharing
Will share

Individual participant data will be uplaoded to a reposiotory hosted by The University of Northampton and will be publicly available online. The DOI and URL to the data set will be included in future publications.

Shared Documents
STUDY PROTOCOL
Time Frame
IPD will be available when the study is published.
Access Criteria
Data underlying the findings of the study will be publicly available via a repository.

Locations