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UnknownNCT05976477

Reduction Of Dietary Salt Intake To Control Systolic Blood Pressure In Hypertensive Older Patients

Reduction Of Dietary Salt Intake To Control Systolic Blood Pressure In Hypertensive Older Patients: The Repress Randomized Controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
266 (estimated)
Sponsor
Mario Negri Institute for Pharmacological Research · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Accepted

Summary

REPRESS is an open label, pragmatic, multicenter, randomized controlled phase III trial with blinded endpoint with 1:1 (intervention to control arm) allocation ratio. The REPRESS trial is aimed to determine the efficacy of an educational intervention aimed at reducing dietary salt intake in elderly people (60+) with moderate hypertension and exposed to polypharmacy (3+ drugs) in improving systolic BP control compared to an attention arm.

Conditions

Interventions

TypeNameDescription
OTHEReducational intervention1. four short videos (about one-minute/one-minute and half duration) concerning the topic of reducing dietary salt intake to control the blood pressure in elderly hypertensive patients: the mini-videos will be designed with a common thread starting from providing general information regarding diet to enhance awareness of the amount of salt that is usually introduced with the diet, up to give suggestions on which products to choose/avoid during grocery shopping and how to behave during the preparation and consumption of food at home to reduce salt intake; 2. Four images informing participants about the risk of excessive salt intake and health benefits of a low-sodium diet and tips on how to reduce daily salt intake; 3. Four recipes for tasty easy-to-prepare meals, avoiding added salt.

Timeline

Start date
2023-10-01
Primary completion
2025-06-30
Completion
2025-12-31
First posted
2023-08-04
Last updated
2023-09-01

Source: ClinicalTrials.gov record NCT05976477. Inclusion in this directory is not an endorsement.