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Clinical Trials in Canada / NCT07142694
Starting soon Not applicable

Feasibility of Adding a Plant-Based Protein Pudding to the Diet of Older Adults Who Attend a Medically Managed Fitness Facility

NCT07142694 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2026-01-15
Last updated
2026-02-05

Condition(s) studied

Feasibility StudiesNutrition Intervention

Investigational drug(s) / intervention(s)

Plant Based pudding

Plant Based pudding: Will consume one high protein plant based pudding daily for 7-days per week for 12 weeks

Study summary

The goal of this a 12-week randomized controlled parallel arm feasibility trial is to evaluate the feasibility and acceptability of incorporating a plant-based protein pudding into the diets of older adults who attend a medically managed fitness facility. The primary participant population includes older adults, aged 60 years and above, who are generally healthy and engaged in structured fitness programs.

The main questions it aims to answer are:

Is a plant-based protein pudding acceptable and well-tolerated by older adults? Does regular consumption of the pudding support muscle health and overall well-being in this population?

Participants will:

Consume a plant-based protein pudding as one arm daily for 7 days per week (experimental) and the other will continue their current lifestyle (control).

The experimental group will complete surveys or questionnaires to assess acceptability, taste, and ease of integration into daily meals.

Undergo basic physical or health assessments (e.g., muscle function or strength evaluations) to evaluate potential effects.

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Participant is willing and able to give informed consent for participation in the trial * Male or female aged ≥60 years * Actively attend the Wellness Institute (≥8 times in the past 28 days), Exclusion Criteria: * Allergy to ingredients in the study treatment * Inability to consume treatment product * Inability to obtain written informed consent * Apart of any physical rehab program at WI (cardiac rehab, kidney fit, etc. )

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chronic Disease Innovation Centre Winnipeg Manitoba

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07142694 on ClinicalTrials.gov ↗ ← All trials in Canada