ELLIDA: Adaptive Training Recommendations for Improved Physical Performance

Sponsor
The Swedish School of Sport and Health Sciences (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06145152
Collaborator
Silicon Valley Exercise Analytics (svexa) (Other)
40
1
2
24
1.7

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Adaptive exercise training
  • Procedure: Static exercise training
Phase 1

Detailed Description

40 recreational athletes, 20 male and 20 females, will be recruited to this study. The research subjects will be stratified into two groups: an Adaptive and a Static training group. The training sessions will be mainly home-based training according to daily instructions from an online application. Testing sessions will be performed on a laboratory treadmill. During the entire period (run-in + training period) the participants will wear continuous glucose monitors for minute-by-minute glucose tracking, an Oura ring for sleep measurements, a Garmin GPS watch with heart rate chest-strap for training data and answer questiions regarding subjective well-being using an online application (Readiness Advisor).

The training program will be a mixture of training sessions based on the experience levels of the research subject.

During the onboarding session, data from each persons Garmin watch, will be used to create an optimal training program that takes into account recent training history and which type of training each subject responds the best to. For the subjects in the Adaptive group the training will be adjusted up or down on a daily basis based on subjective readiness, sleep or glucose control. The subjects in the Static group will not get any adjustments in their training program regardless of readiness level.

The length of the training intervention will be 8 weeks.

In addition to adjusting the training for the adaptive group based on daily readiness, the training in that group will be adjusted based on actual training done. For example if a participant fails to reach his suggested heart rate range during a prescribed session, the training load for upcoming sessions will be recalculated so that the weekly overall training load goal is achieved. This kind of adjustments will not be done in the static training group.

Both pre and post the training period a battery of physiological tests will be done including determination of VO2max, lactate threshold and running economy. A performance test (3000m time-trial) will be done on a running track.

A muscle biopsy will be donated from the Vastus Lateralis for assessment of mitochondrial function, efficiency, capacity and density using a combination of methods including respirometry, western blot and enzymatic methods. Capillarization and number of myonuclei will be assessed using histochemical staining. In addition muscle buffering capacity will be investigated using an acid-titration assay.

In addition to the physiological and biochemical investigation, parameters such as subjective training tolerability, perceived pleasure of the training and number of dropouts are important objectives in the proposed studie.

Statistical power calculation. Based on the parallel group design, 80% power, an alpha of 0.05 and a coefficient of variation of 2.4% for VO2max, 4.2% for performance and 14% for mitochondrial function, a differences can be detected between groups of 6%, 11% and 26% for the three outcomes if 15 participants per group are included. 20 subjects will be recruited per group to allow for 5 dropouts per group.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Basic Science
Official Title:
Using AI-generated Adaptive Training Recommendations to Improve Physical Performance
Anticipated Study Start Date :
Dec 1, 2023
Anticipated Primary Completion Date :
Jul 1, 2025
Anticipated Study Completion Date :
Dec 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Adaptive

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

Procedure: Adaptive exercise training
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)

Active Comparator: Static

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

Outcome Measures

Primary Outcome Measures

  1. Physical performance [pre intervention and within 5 days post intervention]

    3000 meter time trial performance

Secondary Outcome Measures

  1. Maximal oxygen consumption [pre intervention and within 5 days post intervention]

    maximal oxygen consumption at the end of an incremental exercise stress test

  2. Lactate threshold [pre intervention and within 5 days post intervention]

    lactate threshold (anaerobic threshold) as assessed by blood lactate concentration during a submaximal running test on the treadmill

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 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)

Exclusion Criteria:
  • Heart, lung or metabolic disease

  • Recurrent running injuries

  • Not willing to use wearable devices

  • Performing a subtantial amount of non-running exercise training

Contacts and Locations

Locations

Site City State Country Postal Code
1 Swedish School of Sports and Health Sciences Stockholm Sweden 114 86

Sponsors and Collaborators

  • The Swedish School of Sport and Health Sciences
  • Silicon Valley Exercise Analytics (svexa)

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Filip Larsen, Associate Professor, The Swedish School of Sport and Health Sciences
ClinicalTrials.gov Identifier:
NCT06145152
Other Study ID Numbers:
  • Ellida
First Posted:
Nov 22, 2023
Last Update Posted:
Nov 22, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Filip Larsen, Associate Professor, The Swedish School of Sport and Health Sciences

Study Results

No Results Posted as of Nov 22, 2023