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ACTIVE NOT RECRUITING
NCT06764121
NA

Impact of Canadian Haskap Berry Powder on Hypertension and Acuity in Women's Health

Sponsor: University of Manitoba

View on ClinicalTrials.gov

Summary

Haskap berries are rich in cyanidin-3-O-glucoside (C3G), which has been shown in vitro to enhance endothelial function. Previous clinical studies suggest haskap berry supplementation may improve cognition, mood, blood pressure, and athletic performance, but research is limited. This trial aims to contribute to the growing body of evidence on the effects of haskap berry supplementation. The trial is a 2-period, randomized, double-blinded, cross-over design lasting 16 weeks. During the first period (weeks 0-6), participants will receive either haskap berry powder or a control powder. A 4-week washout period follows (weeks 7-10), where no powder is consumed. In the second period (weeks 11-16), participants will receive the powder they did not consume in the first period.

Official title: Impact of Haskalife(TM) Canadian Haskap Berry Powder Formulation on Hypertension and Acuity in Women's Health

Key Details

Gender

FEMALE

Age Range

35 Years - Any

Study Type

INTERVENTIONAL

Enrollment

32

Start Date

2025-04-03

Completion Date

2026-08-06

Last Updated

2025-12-04

Healthy Volunteers

No

Interventions

OTHER

Haskap Berry Powder

The participants will consume four packets (16g) of haskap berry powder. The powder can be consumed with other food products.

OTHER

Placebo Powder

The participants will consume four packets (24g) of placebo powder. The powder can be consumed with other food products.

Locations (1)

Richardson Centre for Food Technology and Research

Winnipeg, Manitoba, Canada