NCT06145152

Brief Summary

In this study two different training strategies are compared; one is adaptive where the training is adjusted up or down on a daily basis to better match the recovery status (readiness) of the subject. The other strategy is static, i.e. no changes are made depending on readiness level. Instead the subjects in the static group are encouraged to perform the prescribed training. The training intervention will last for 8 weeks. Thorough physiological tests will be performed pre and post the training intervention together with muscle biopsies for assessment of mitochondrial function.

Trial Health

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Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P50-P75 for phase_1

Timeline
Completed

Started Dec 2023

Typical duration for phase_1

Geographic Reach
1 country

1 active site

Status
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

November 6, 2023

Completed
16 days until next milestone

First Posted

Study publicly available on registry

November 22, 2023

Completed
13 days until next milestone

Study Start

First participant enrolled

December 5, 2023

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2025

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

March 20, 2024

Status Verified

March 1, 2024

Enrollment Period

1.6 years

First QC Date

November 6, 2023

Last Update Submit

March 18, 2024

Conditions

Keywords

exerciseAI

Outcome Measures

Primary Outcomes (1)

  • Physical performance

    3000 meter time trial performance

    pre intervention and within 5 days post intervention

Secondary Outcomes (2)

  • Maximal oxygen consumption

    pre intervention and within 5 days post intervention

  • Lactate threshold

    pre intervention and within 5 days post intervention

Study Arms (2)

Adaptive

EXPERIMENTAL

Subjects in the Adaptive group will get updated and adjusted training programs based on daily readiness level

Procedure: Adaptive exercise training

Static

ACTIVE COMPARATOR

Subjects in the Static group will get the same inital training program as the Adaptive group but will not get updated and adjusted training programs based on daily readiness level

Procedure: Static exercise training

Interventions

The training recommendation for the day will be adjusted based on the readiness level. The adjustments can be both up or down (increased or decreased training)

Adaptive

The training recommendation for the day will not be adjusted based on the readiness level.

Static

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Training history of at least two running sessions per week (5km +) the last 6 months
  • No chronic diseases
  • Able to perform maximal exercise
  • Having used a smart watch for training frequently during the last 3 months
  • Willing to use wearable technology (Oura ring, continuous glucose monitor, running GPS watch)

You may not qualify if:

  • Heart, lung or metabolic disease
  • Recurrent running injuries
  • Not willing to use wearable devices
  • Performing a subtantial amount of non-running exercise training

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Swedish School of Sports and Health Sciences

Stockholm, 114 86, Sweden

RECRUITING

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Design

Study Type
interventional
Phase
phase 1
Allocation
NON RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

November 6, 2023

First Posted

November 22, 2023

Study Start

December 5, 2023

Primary Completion

July 1, 2025

Study Completion

December 1, 2025

Last Updated

March 20, 2024

Record last verified: 2024-03

Data Sharing

IPD Sharing
Will not share

Locations