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Lifestyle Intervention for Treating Systemic Hypertension in Primary Care Setting

L

Laval University

Status

Completed

Conditions

Hypertension

Treatments

Behavioral: Lifestyle intervention

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The Canadian hypertension education program recommends increased physical activity, adoption of the Dietary Approaches to Stop Hypertension (DASH) diet, and reduction in sodium and alcohol intake for treatment and prevention of hypertension. Objective: To describe patients participating in an interdisciplinary lifestyle intervention to reduce blood pressure in a family medicine primary care setting. Design: Descriptive study. Participants: The study aims to recruit 60 sedentary hypertensive patients to participate in a 6-month randomized-controlled trial. To be eligible, patients must be ≥18 years of age, sedentary (7-day measured steps/day and self-report), hypertensive (based on 24-h ambulatory blood pressure measurements [ABPM]), non-smoker, non-diabetic and without dyslipidemia. Intervention: Patients are recruited by health care professionals of the family medicine unit and are thereafter randomized to one of four intervention groups: 1) standard medical care (control), 2) improved diet (DASH diet), 3) physical activity, or 4) both improved diet and physical activity. Patients are evaluated (pre, mid and post intervention), monitored, and educated by the interdisciplinary health care team that includes a physician, a kinesiologist, a nutritionist and a nurse, depending on the intervention group. T-tests and descriptive statistics were used to analyse data. This study will document the efficacy of a primary care lifestyle intervention program on cardiometabolic and hypertension risk factors.

Enrollment

60 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ≥18 years of age
  • Sedentary (7-day measured steps/day and self-report)
  • Arterial hypertensive (based on 24-h ambulatory blood pressure measurements [ABPM])

Exclusion criteria

  • secondary hypertension
  • diabetes
  • dyslipidemia
  • cardiovascular diseases with complications
  • smoker

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

60 participants in 4 patient groups

Physical activity
Experimental group
Description:
Tailoring intervention with kinesiologist
Treatment:
Behavioral: Lifestyle intervention
Diet
Experimental group
Description:
Tailoring intervention with nutritionist
Treatment:
Behavioral: Lifestyle intervention
Physical activity and diet
Experimental group
Description:
Tailoring intervention with kinesiologist and nutritionist
Treatment:
Behavioral: Lifestyle intervention
Standard medical care
No Intervention group
Description:
Follow with family doctor as usual care.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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