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Isometric Handgrip Home Training to Lower Blood Pressure in Hypertensive Older adulTs

Isometric Handgrip Home Training to Lower Blood Pressure in Hypertensive Older adulTs: a 20-week Assessor-blindEd raNdomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03069443
Acronym
POTENT
Enrollment
48
Registered
2017-03-03
Start date
2017-03-15
Completion date
2020-07-09
Last updated
2020-07-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Isometric handgrip training, home training, older adults, Hypertension

Brief summary

This Study evaluates the effect of 20 weeks of isometric handgrip (IHG) home training in adults aged 50 years or more. Half of the participants will serve as a control group and will only receive hypertension-guidelines on lifestyle changes.

Detailed description

Hypertension markedly increases the risk of cardiovascular diseases and overall mortality. Lifestyle modifications such as increased levels of physical activity are recommended as the first line of anti-hypertensive treatment. A recent systematic review showed that isometric handgrip (IHG) training was superior to traditional endurance and strength training in lowering resting systolic blood pressure (SBP). The average length of previous IHG training studies is approximately 7.5 weeks with the longest being 10 weeks. Therefore, presently it is unknown if it is possible to further lower blood pressure levels beyond the 10 week mark. Recently, the investigators developed a novel method for monitoring handgrip intensity using a standard Nintendo Wii Board (Wii). The primary aim of this study is to explore the effects of 20-weeks IHG home training facilitated by a Wii in hypertensive older adults (+50 years of age) in lowering SBP compared to usual care. Secondary aims are to explore if/when a leveling off effect on SBP will occur during the 20-week intervention period in the training group and to explore adherence and potential harms related to the IHG home training. Methods: Based on previous evidence, the investigators calculated that 50 hypertensive older adults (+50 years of age) is needed to achieve a power of 80% or more. Participants will be randomly assigned to either an intervention group (IHG home training + hypertension-guidelines on lifestyle changes) or to a control group (hypertension-guidelines on lifestyle changes). Participants in the intervention group will perform IHG home training (30% of maximum grip strength for a total of 8 min per day per hand) three times a week for 20-weeks.

Interventions

OTHERIHG home training

Participants of the intervention group will follow the IHG home training protocol for 20 weeks. The IHG training consists of isometric contractions applied with the hands on a Wii.

Sponsors

Odense University Hospital
CollaboratorOTHER
Aalborg University
CollaboratorOTHER
Aalborg University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to 120 Years
Healthy volunteers
No

Inclusion criteria

1. Age +50 years old 2. Un-medicated (anti-hypertensive medicine) with resting SBP between 135-179 mmHg or hypertensive patient medicated with no change in treatment for ≥ 4 months with resting SBP between 135-179 mmHg

Exclusion criteria

1. Manifest cardiovascular disease (cerebrovascular disease, Heart failure, Chronic Kidney Disease, peripheral vascular disease, and advanced retinopathy (fundus hypertonus III-IV)). 2. Diabetes (any type) 3. More than three blood pressure regulating agents 4. Physical limitation preventing IHG training (e.g. missing an arm or musculoskeletal disorders). 5. Arthritis in the hand or carpal tunnel 6. SBP ≥ 180 mmHg (will be advised to see a doctor)

Design outcomes

Primary

MeasureTime frameDescription
Systolic blood pressureafter 20 weeks of trainingmeasured using a standard hospital electrical sphygmomanometer (Omron Comfort M6 AC)

Secondary

MeasureTime frameDescription
heart rateafter 20 weeks of trainingmeasured using a standard hospital electrical sphygmomanometer (Omron Comfort M6 AC)
Handgrip maximum strengthbaseline, 5 week, 15 weeks, and 20 weeks followupThis will be measured using the WII and reported in kilograms in the FysioMeter software
Handgrip Rate of force developmentbaseline, 5 week, 15 weeks, and 20 weeks followupmeasured using a specially designed software working together with a standard wii board.
Diastolic blood pressureafter 20 weeks of trainingmeasured using a standard hospital electrical sphygmomanometer (Omron Comfort M6 AC)
Visual Analog Pain Scale (VAS)after 20 weeks of trainingAt the end of each training session. Pain will be assessed for each hand/side using the VAS scale
Compliance to training sessionsafter 20 weeks of trainingA report will be generated on how many sessions each participant have completed during the study
Systolic blood pressureweek 25, 35, and 40 post-interventionmeasured using a standard hospital electrical sphygmomanometer (Omron Comfort M6 AC)
Handgrip Force variabilityafter 20 weeks of trainingThis will be a measure of the muscle force variability during the isometric training sessions throughout the study

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026