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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

Evaluation of a Plant-based Protein Pudding In Older Adults Attending a Medically Managed Fitness Facility

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07142694
Enrollment
40
Registered
2025-08-27
Start date
2026-01-15
Completion date
2026-05-01
Last updated
2026-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Feasibility Studies, Nutrition Intervention

Brief 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.

Interventions

DIETARY_SUPPLEMENTPlant Based pudding

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

Sponsors

Seven Oaks Hospital Chronic Disease Innovation Centre
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

This trial is a randomized controlled parallel arm feasibility trial

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

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. )

Design outcomes

Primary

MeasureTime frameDescription
Eligibility to Randomization Ratio for FeasibilityMeasured upon study completion after 12-weeksA ratio of eligibility to randomization will be collected at 12 months. The trial will be considered feasible if ratio falls within \>0.5, calculated as the ratio of individuals who were randomized to the trial to the number eligible to participate who were approached to participate.
Recruitment Rateduring 12 monthsRecruitment rate will be assessed as the average number of new participants enrolled per site per week during the active recruitment period, with a target of ≥0.5 participants per site per week.
Follow up rateMeasured at end of 12 weeksFollow-up rate (% of participant outcomes) will be calculated if more than \>85% of participant outcomes
Adherence to InterventionMeasured at the end of 12 weeksAdherence to plant based pudding intervention if more than (75% of dispensed plant based pudding protein is consumed)

Secondary

MeasureTime frameDescription
Serum Pre-AlbuminMeasured at Baseline Week 1 and at the end of 12 weeks.Serum albumin is measured in grams per deciliter (g/dL)
Blood Amino Acid ProfileMeasured at Baseline Week 1 and at the end of week 12blood amino acid profile
Dry WeightMeasured at Baseline Week 1 and after the end of week 12Changes in body weight (Kg)
Waist CircumsferenceMeasured at Baseline Week 1 and after the end of week 12Measured in cm
Lean massAt the baseline week 1 and at end of week 12Measured in Kg
Fat MassAt the baseline week 1 and at end of week 12Measured in Kg
Physical function; Five rep chair stand time testMeasured at Baseline Week 1 and after the end of week 12the amount of time it takes for a participant to get up out of a chair five times measured in seconds
Blood PressureMeasured at Baseline Week 1 and after the end of week 12Systolic and Diastolic Blood Pressure Measured in mmHg
Total Calories intakeMeasured at Baseline Week 1 and after the end of week 12Using RxFoods- Diet recall change in total calories measured in kcal/day
CarbohydratesAt the baseline week 1 and at end of week 12Measured as g/day
ProteinAt the baseline week 1 and at end of week 12Measured as g/day
FatAt the baseline week 1 and at end of week 12Measured as g/day
Fiber (total dietary fiber)At the baseline week 1 and at end of week 12Measured as g/day

Countries

Canada

Contacts

CONTACTNavdeep Tangri Dr. Tangri, MD, PhD
NTangri@sogh.mb.ca204-631-3834
CONTACTMaryem Zahra, BA
MZahra@sogh.mb.ca204-631-3834

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026