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

A

Anil Nigam

Status

Unknown

Conditions

Hypertension,Essential
Exercise Activity

Treatments

Other: 24h-Ambulatory Blood Pressure

Study type

Interventional

Funder types

Other

Identifiers

NCT04103411
2018-2319

Details and patient eligibility

About

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.

Enrollment

60 estimated patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

High Intensity Interval Training (HIIT)
Experimental group
Description:
For the twelve weeks of intervention, participants will have three training sessions per week. Each session will be done on a cycle ergometer and will last approximately 40 minutes. Participants will be supervised by certified kinesiologists and their training programs will be revised every four weeks.
Treatment:
Other: 24h-Ambulatory Blood Pressure
HydroChloroThiazide
Active Comparator group
Description:
For this group, participants have to take a diuretic (12,5 mg of Hydrochlorothiazide) daily prescribed by the doctor of this study, for twelve weeks. Participants should also maintain the same lifestyle habits that they had before the study.
Treatment:
Other: 24h-Ambulatory Blood Pressure

Trial contacts and locations

1

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Central trial contact

Antoine Langeard, PhD; Anil Nigam, MD

Data sourced from clinicaltrials.gov

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