ClinicalTrials.gg
CompletedNCT06662487Updated Oct 30, 2024

The Effect of Free Weight Resistance Training and Body Composition on Cognition

An interventional study of Resistance Training in Cognitive Performance, sponsored by Pontificia Universidad Catolica de Valparaiso. Completed at 1 site in Chile. Open to participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-10-30.

Sponsored by Pontificia Universidad Catolica de Valparaiso · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 1 month after the study started (first participant enrolled Sep 2023, registered Oct 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

This study, titled The Effect of Free Weight Resistance Training (FWRT) on Cognitive Function Explored through Eye Tracking, will be a randomized double-blind clinical trial aimed at evaluating how FWRT influences cognitive processing in healthy young adults. Eye-tracking technology will be used to measure reading metrics and DXA scans will be used to measure body composition before and after a 10-week FWRT intervention.

Participants will be randomly assigned to either an experimental group, which will undergo a 10-week FWRT program, or a control group. This study will provide insights into the potential benefits of free weight resistance training on the cognitive performance of text processing tasks.

02

Conditions studied

  • Cognitive Performance
03

In context

Lead sponsor

Pontificia Universidad Catolica de Valparaiso is the lead sponsor of 7 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • University students between the ages of 18 and 30.
  • Healthy individuals with no recent participation (last six months) in physical training programs.
  • Normal or corrected-to-normal vision.

Exclusion criteria

Exclusion Criteria:

  • Physical or health limitations that prevent participation in a resistance training program.
  • Current involvement in other physical training programs.
  • Visual impairments that cannot be corrected with glasses or contact lenses.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
12 participants (actual)

Study arms

  • Experimental
    Free Weight Resistance Training (FWRT)

    Participants in the experimental group will engage in a 10-week free weight resistance training program. This program will consist of 3 weekly sessions, including exercises such as squats, deadlifts, and bench presses, among others. The training will focus on progressively increasing the intensity, working within a range of 60% to 80% of the one-repetition maximum (1RM).

    Behavioral: Resistance Training

  • No intervention
    Control Group

    Participants in the control group will not receive any intervention and will be instructed to continue with their usual daily routine. These participants will be evaluated pre- and post-intervention in the same manner as the experimental group but will not participate in the training program.

Interventions

  • BehavioralResistance Training

    Participants in the experimental group will perform free weight resistance training sessions focused on push, pull, and leg movement patterns. The program will last for 10 weeks, progressively increasing in load and intensity. The intervention will be designed to improve the participants' physical strength and observe how these changes affect their cognitive performance.

06

What researchers measure

Primary outcomes

  1. Cognitive Measures (Eye-Tracking Metrics)

    Cognitive metrics (as text processing metrics) will be measured through an eye-tracking device (EyeLink Portable Duo), with the following key metrics: * First Pass Reading Times: Total time spent on fixations during the first pass of reading within an area of interest. * Total Reading Times: The sum of the durations of all fixations within an area of interest, including revisits to previously read areas. * Other eye-tracking or comprehension measures could also be used.

    Time frame: Up to 10 weeks post-intervention

07

Study locations

1 site
  • Pontificia Universidad Católica de Valparaíso,
    Valparaíso, Chile
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 30, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06662487
Lead sponsor
Pontificia Universidad Catolica de Valparaiso
Responsible party
Carlos Cristi Montero (Head of Investigation, Pontificia Universidad Catolica de Valparaiso) — Principal investigator
First posted
Oct 29, 2024
Start date
Sep 1, 2023
Primary completion
Aug 30, 2024
Completion
Oct 20, 2024
Last update
Oct 30, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2024. You cannot join it, but the record below documents what was studied.

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