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NOT YET RECRUITING
NCT07882706
NA

Effect of Aerobic Training Supported by AI-Based Monitoring on Functional Performance in University Students With Anemia

Sponsor: Cairo University

View on ClinicalTrials.gov

Summary

This study aims to examine the impact of aerobic training supported by AI-based monitoring on functional performance in university students with anemia.

Key Details

Gender

All

Age Range

18 Years - 25 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2026-10-30

Completion Date

2028-10-30

Last Updated

2026-10-20

Healthy Volunteers

No

Conditions

Interventions

BEHAVIORAL

Aerobic Treadmill Training

Participants in the experimental group will perform supervised moderate-intensity aerobic treadmill training three times per week for 12 weeks. Each 30-minute session will include a 5-minute warm-up, 20 minutes of treadmill walking at 60-70% of maximum heart rate (HRmax = 220 - age), and a 5-minute cool-down. Treadmill speed and/or incline will be individually adjusted to maintain the target intensity. Exercise progression will be guided by heart rate, perceived exertion, fatigue, symptoms, and weekly AI-assisted monitoring, with all clinical decisions made by the supervising physical therapist.

BEHAVIORAL

AI-Supported Adaptive Cognitive Training

Participants in the experimental group will receive adaptive digital cognitive training using the BrainHQ application three times weekly for 12 weeks, alongside aerobic treadmill training. The program will include computerized cognitive exercises targeting attention, processing speed, and working memory. Task difficulty and training progression will be adapted according to individual performance to provide personalized cognitive stimulation. Training adherence and tolerance will be reviewed regularly by the researcher. Cognitive performance will be assessed before and after the intervention using the Trail Making Test (TMT) mobile application.

OTHER

Standard Care for Anemia

Participants in both groups will receive standard care for anemia throughout the 12-week study period, including usual medical and nutritional advice. Any physician-prescribed iron supplementation or other medications will be documented. Standard care will be provided alongside the assigned intervention in the experimental group, while participants in the control group will receive standard care without structured aerobic training or AI-supported cognitive training.

Locations (1)

Delta University for Science and Technology

Gamasa, Egypt