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

NCT07142694 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2026-02-05

No results posted yet for this 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.

Conditions

  • Feasibility Studies
  • Nutrition Intervention

Interventions

DIETARY_SUPPLEMENT

Plant Based pudding

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

Sponsors & Collaborators

  • Seven Oaks Hospital Chronic Disease Innovation Centre

    lead NETWORK

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-01-15
Primary Completion
2026-04-15
Completion
2026-05-01

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07142694 on ClinicalTrials.gov