The UBC Long-distance Triathlon Adaptation Study

NCT ID: NCT06467656

Last Updated: 2025-04-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-20

Study Completion Date

2026-01-30

Brief Summary

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The purpose of this study is to investigate the effect of 12-months of individualized endurance-training (swimming, cycling and running) on physiological and psychological adaptations in exercise naïve individuals. Due to the potential seasonal changes that naturally occur in individuals across a year (even without training) the investigators will also compare the exercise-trained group to a time-aligned control group.

Detailed Description

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Endurance training is well-accepted to lead to numerous positive physiological and psychological adaptations. However, many of the previous studies examining the benefits of endurance exercise on the human body have: 1) compared athletes with non-athletes using a cross-sectional design, 2) have employed training studies that are relatively short (e.g. weeks to months) in duration, 3) have primarily focused on male participants and not examined potential sex-differences, and 4) have not specifically recruited exercise naïve participants, as often participants are already engaged in ongoing recreational or competitive activities at the time of recruitment. As such, we have a limited understanding of the true time-course of adaptations that occur in exercise naïve individuals in response to training, or how physiological and psychological adaptations change beyond 4-6 months, and whether there are sex-specific differences in these adaptations.

This study is primarily designed to determine the time-course of adaptation and remodeling in females and males across multiple different physiological systems (i.e. cardiac, vascular, metabolic, respiratory, immune, and microbiome) and psychological measures at rest and in response to a range of provocations.

Forty healthy exercise-training naïve individuals (20 females: 20 males) will perform 12-months of individually prescribed, endurance training (including supplementary strengthening exercise for conditioning and injury prevention) designed to prepare participants for an ultra-endurance triathlon. A time-aligned control group of 20 healthy exercise-training naïve individuals (10 females: 10 males) will also be recruited to determine the natural change that occurs in each system across a year. Outcomes will be assessed at baseline, 3 months, 6 months and 12 months. Additionally, cardiovascular outcomes will also be assessed at 1 month and immune outcomes will be repeated at 3 months post intervention (15 months).

Conditions

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Healthy Participants

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

This will be a parallel group, non-randomized study.
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Exercise Intervention

Participants will engage in 12 months of individualized endurance-training (swimming, cycling and running) and 9 months of supplemental strengthening exercises. Exercise prescriptions will be provided to participants weekly via an app (TrainingPeaks). Sessions will vary in length from 30 min to 8 hours throughout the program.

Group Type EXPERIMENTAL

Individualized, periodized endurance training for ultra-endurance triathlon.

Intervention Type OTHER

Endurance exercise consisting of swimming, cycling and running training for a minimum of 3 hours /week up to a maximum of 20 hours/week with regular rest days and intensities being fluctuated throughout the program to optimize training stimulus and adaptation. Strengthening exercises to complement the aerobic training, enhance conditioning and prevent injury will also be performed 1-2 hours/week for the first 9-months of the program.

Time-Aligned Control

Participants in the control arm will continue to live their lives exactly as they would if they were not enrolled in a study to allow evaluation of natural biological changes that occur across 12-months of free-living.

Group Type ACTIVE_COMPARATOR

Time-Aligned Control

Intervention Type OTHER

Participants will receive no specific intervention and will continue to live their lives as if they were not in a study.

Interventions

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Individualized, periodized endurance training for ultra-endurance triathlon.

Endurance exercise consisting of swimming, cycling and running training for a minimum of 3 hours /week up to a maximum of 20 hours/week with regular rest days and intensities being fluctuated throughout the program to optimize training stimulus and adaptation. Strengthening exercises to complement the aerobic training, enhance conditioning and prevent injury will also be performed 1-2 hours/week for the first 9-months of the program.

Intervention Type OTHER

Time-Aligned Control

Participants will receive no specific intervention and will continue to live their lives as if they were not in a study.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Aged 19-39 years
* Non-smoker (quit \>6 months)
* Able to swim \>100 meters without stopping
* Have access to, or willingness, to obtain a road bicycle
* Are willing to commit to the research assessments and prescribed training program
* Currently performing \<120 minutes of structured endurance training per week
* Premenopausal


* Aged 19-39 years
* Non-smoker (quit \>6 months)
* Are willing to commit to the research assessments
* Currently performing \<120 minutes of structured endurance training per week
* Premenopausal

Exclusion Criteria

* History of heart disease
* History of lung disease (not including controlled asthma)
* History of metabolic disease
* History of cancer
* Chronic inflammatory conditions
* Blood pressure \> 140/90 mmHg
* Chronic antibiotic, antiviral, antimicrobial, non-steroidal anti-inflammatory drugs (NSAIDs) and antihistamine use
* Are a regular (more than 1/week) cannabis user
* Consume alcohol regularly: more than 6 standard drinks per week (e.g.14-20 ounces of beer and 5-8 ounces of wine)
* Have previously completed structured endurance exercise training for an extended period of time (such as training for a triathlon or running race)
* Have previously participated in competitive team sports with an aerobic component (e.g. soccer, basketball, rugby, field hockey) and sport-specific training (e.g. hockey, football) \>3 times per week within the previous 5 years
* Have prior experience of heavy structured resistance training \>3x/week within the last 2 years
* BMI\>32 kg/m2 or \<20 kg/m2
* Pregnancy within 12 months, or planning to become pregnant within the next 12 months
* Currently breast feeding (or having stopped within 6 months)
* Planning to be away from the Okanagan area for an extended period over the duration of the study
Minimum Eligible Age

19 Years

Maximum Eligible Age

39 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of British Columbia

OTHER

Sponsor Role lead

Responsible Party

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Robert Shave

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Robert Shave, PhD

Role: PRINCIPAL_INVESTIGATOR

University of British Columbia

Locations

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University of British Columbia

Kelowna, British Columbia, Canada

Site Status RECRUITING

Countries

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Canada

Central Contacts

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Robert Shave, PhD

Role: CONTACT

250-317-7226

Neil Eves, PhD

Role: CONTACT

250-807-9676

Other Identifiers

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H24-00882

Identifier Type: -

Identifier Source: org_study_id

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