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Clinical Trials/NCT02920437
NCT02920437TerminatedNot Applicable

A Pilot Randomized Controlled Trial to Reduce Salt Intake Among Hypertensive Young Adults in Hong Kong

The University of Hong Kong1 site in 1 country19 target enrollmentStarted: October 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
19
Locations
1
Primary Endpoint
24-hour urinary sodium excretion

Study Overview

Brief Summary

A pilot randomized controlled trial will be conducted to investigate the feasibility and effectiveness of a salt intake reduction intervention to young hypertension patients in Hong Kong who had high salt intake.

Detailed Description

Convenience sample will be recruited from the community in Hong Kong through different channels of promotion.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 44 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •i) adults aged 18 to 44
  • •ii) diagnosed hypertension or borderline hypertension
  • •iii) complete collection of 24-hour urine at baseline
  • •iv) 24-hour urinary sodium excretion above 2000mg at baseline
  • •v) can communicate in Cantonese

Exclusion Criteria

  • •i) renal illnesses;
  • •ii) taking diuretics;
  • •iii) taking RAS blockers;
  • •iv) attending or planning to attend new hypertension education programme or salt intake reduction programme during the study period.

Arms & Interventions

Intervention group

Experimental

Four-week weekly intervention to reduce salt intake.

Intervention: Four-week weekly intervention to reduce salt intake (Behavioral)

Control group

Other

Usual government pamphlets.

Intervention: Usual government pamphlets (Other)

Outcomes

Primary Outcomes

24-hour urinary sodium excretion

Time Frame: 10-Week

Difference between the intervention and control group in the change in 24-hour urinary sodium excretion from baseline to the end of follow-up

Secondary Outcomes

  • Health literacy on low salt intake(10-Week)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr. Pui-Hing Chau

Assistant Professor

The University of Hong Kong

Study Sites (1)

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