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Effect of High-Intensity Interval Training Compared to Hydrochlorothiazide on Ambulatory Blood Pressure

Effect of High-Intensity Interval Training Compared to Hydrochlorothiazide on Ambulatory Blood Pressure, Cardiovascular Health, Cognition and Mobility in Pre-Hypertensive Older Adults.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04103411
Acronym
DIISCCO
Enrollment
60
Registered
2019-09-25
Start date
2018-04-26
Completion date
2022-01-10
Last updated
2019-09-25

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

Conditions

Exercise Activity, Hypertension,Essential

Brief summary

The number of persons with hypertension is increasing and with it the number of related cardiovascular events and related functional or cognitive declines. While studies have suggested that physical activity, in particular, high-intensity interval training (HIIT), could be as efficient as the commonly used antihypertensive medications, no studies have actually compared their effects in the same population. This protocol will determine if HIIT is at least as efficient as hydrochlorothiazide in order to lower 24h-ambulatory blood pressure (BP) in prehypertensive older adults.

Interventions

OTHER24h-Ambulatory Blood Pressure

Effect of High Intensity Interval Training compared to Hydrochlorothiazide on ambulatory Blood Pressure.

Sponsors

Anil Nigam
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Age at consent ≥ 60 years; 2. Systolic Blood pressure measured through BPtru™ between SBP ≥ 120 mmHg and \< 140 and or DBP ≥ 80 mmHg 3. Being able to sign the informed consent form

Exclusion criteria

1. Considered highly active according to the International Physical Activity Questionnaire 2. Practicing more than 20 min per week of High-Intensity Interval Training 3. Use of antihypertensive medication 4. Contraindication for the practice of intense physical activity 5. Functional limitations related to the exercise test and to intensive training 6. Cardiovascular pathology 7. Atrial fibrillation 8. Psychiatric or neurological disorder 9. Renal failure 10. MMSE score \< 26 11. Persons benefiting of enhanced protection: persons deprived of their liberty by a judicial or administrative decision, persons staying in a health or social institution, adults under legal protection and patients in emergency situations. 12. Diabetes

Design outcomes

Primary

MeasureTime frameDescription
24h-Ambulatory Blood PressureAt baseline and after twelve weeks of interventionThe 24-hour ambulatory measure of the blood pressure (AMBP)

Secondary

MeasureTime frameDescription
Flow Mediated Dilatation (FMD)Before and after twelve weeks of interventionPercentage of dilatation of the brachial artery
Cardiovascular evaluationBefore and after twelve weeks of interventionMaximum incremental cardiopulmonary exercise test (VO2MAX)
Cognitive functionsBefore and after twelve weeks of interventionCognitive functions will be measured at rest with a pen-paper battery test by a neuropsychologist. The investigators will measure change of score to the cognitive tests.

Countries

Canada

Contacts

Primary ContactAnil Nigam, MD
anil.nigam@icm-mhi.org514-376-3330
Backup ContactAntoine Langeard, PhD
langeard.antoine@hotmail.fr514-374-1480

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026