ClinicalTrials.Veeva

Menu

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

P

Pontificia Universidad Catolica de Valparaiso

Status

Completed

Conditions

Cognitive Performance

Treatments

Behavioral: Resistance Training

Study type

Interventional

Funder types

Other

Identifiers

NCT06662487
BIOEPUCV-HB 546-2022

Details and patient eligibility

About

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.

Enrollment

12 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

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

  • 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.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

12 participants in 2 patient groups

Free Weight Resistance Training (FWRT)
Experimental group
Description:
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).
Treatment:
Behavioral: Resistance Training
Control Group
No Intervention group
Description:
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.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems