NCT07760597

Brief Summary

Resistance training (RT) is important for building and maintaining healthy muscles. An exercise frequency called "exercise snacks" involves short bursts of exercise throughout the day (\~5-15 minutes), but no studies have examined a gym-based RT exercise snack program. The invetigators will randomize 40 participants into one of two groups for 10 weeks: the control group will complete two full-body workouts per week (standard-frequency) and the experimental group will complete 10 mini-workouts per week (high-frequency). Muscle hypertrophy (size) and strength will be measured before and after the exercise program to determine if the participants had the same or different results.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
9mo left

Started Sep 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 7, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 12, 2026

Completed
20 days until next milestone

Study Start

First participant enrolled

September 1, 2026

Expected
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2027

Last Updated

August 12, 2026

Status Verified

August 1, 2026

Enrollment Period

9 months

First QC Date

August 7, 2026

Last Update Submit

August 7, 2026

Conditions

Keywords

Exerise SnacksExercise FrequencyResistance TrainingMuscle StrengthSkeletal Muscle EnlargementExercise

Outcome Measures

Primary Outcomes (1)

  • Change in Total Body Skeletal Muscle Mass Measured using the D3-Creatine Dilution Method

    From enrolment (Week 1) to the end of the exercise training phase (Week 12)

Secondary Outcomes (4)

  • Change in Total Body Muscle Size Measured as Cross-sectional Area using Muscle Ultrasound Imaging

    From enrolment (Week 1) to the end of the exercise training phase (Week 12)

  • Change in Muscle Strength Measured as the One-Repetition Maximum of Back Squat and Bench Press

    From enrolment (Week 1) to the end of the exercise training phase (Week 12)

  • Change in Skeletal Muscle Power Measured at Various Relative Loads for Back Squat and Bench Press

    From enrolment (Week 1) to the end of the exercise training phase (Week 12)

  • Participant Satisfaction with the Exercise Program

    At the end of the exercise training phase (Week 12)

Study Arms (2)

Standard-frequency resistance training

ACTIVE COMPARATOR
Behavioral: Two sessions per week of resistance training

High-frequency resistance training

EXPERIMENTAL
Behavioral: 10 sessions per week of resistance training

Interventions

Full-body resistance training consisting of 10 sets per week for all major muscle groups with progressive overload in a gym-based setting. Training at an exercise frequency of 10 brief sessions per week (around 8-12 minutes per session).

High-frequency resistance training

Full-body resistance training consisting of 10 sets per week for all major muscle groups with progressive overload in a gym-based setting. Training at an exercise frequency of two sessions per week (around 45-60 minutes per session).

Standard-frequency resistance training

Eligibility Criteria

Age19 Years - 39 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Can fluently read and write in English
  • Lives, works, and/or studies at or near the Gateway Health Building (where all study visits will occur)
  • Willing and able to commit to 2 or 10 in-person training sessions per week for 10 continuous weeks, as well as one week of testing before the training period and one week of testing after the training period
  • Has continuous access to smartphone or other device that they can use to access the Technogym app
  • Answers "No" to all questions on the Canadian Society for Exercise Physiology - Get Active Questonnaire (CSEP-GAQ) or has their doctor's approval to participate

You may not qualify if:

  • Any major uncontrolled cardiovascular, muscular, metabolic, and/or neurological disorders
  • Lung disease, kidney disease, or liver disease
  • Current diagnosis of type 1 diabetes, type 2 diabetes, or cancer
  • Medical conditions that limit their ability to undertake strenuous physical activity
  • Regular use of any medications that may affect muscle physiology or body composition (i.e. benzodiazepines, hormone replacement therapy, ADHD medication, Metformin, Ozempic)
  • Participated in consistent resistance exercise training more than twice per month in the previous 12 months
  • Participated in consistent moderate or vigorous aerobic training more than twice per week in the previous 12 months, or planning to start consistent training in the next few months
  • Significant gain or loss of body mass in the past 6 months (greater than 2 kg)
  • Current smoker (including but not limited to cigarettes, e-cigarettes, or vaping)
  • Body Mass Index of less than 18 kg/m2 or over 30 kg/m2
  • Pregnancy or breastfeeding
  • Currently taking blood thinners
  • Allergic to Tegaderm medical tape (used with the activity trackers)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of British Columbia | Gateway Health Building

Vancouver, British Columbia, V6T 1Z1, Canada

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Central Study Contacts

Cameron Mitchell, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
The person conducting the analysis for cross-sectional area of the muscle ultrasound images will be blinded to participant identity and participant group assignment during this analysis.
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: At the beginning of the study, participants are assigned to one of two groups for the duration of the study.
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

August 7, 2026

First Posted

August 12, 2026

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

June 1, 2027

Study Completion (Estimated)

June 1, 2027

Last Updated

August 12, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

The dataset will contain potentially identifying information (age, height, and weight) of people in a relatively small geographic area, so individual participant data will not be shared with other researchers.

Locations