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Effectiveness of a Home-based Telehealth Exercise Program on Adherence and Performance in Handball Players

C

CEU San Pablo University

Status

Completed

Conditions

Healthy

Treatments

Other: Specific exercise program
Other: General exercise program

Study type

Interventional

Funder types

Other

Identifiers

NCT06900309
CEU-029

Details and patient eligibility

About

The objective of this clinical trial is to determine whether Physitrack®, a telerehabilitation platform, improves players' adherence to exercise programs. The secondary objectives are to assess whether its use enhances players' jumping ability (speed, height, flight time) and to evaluate the usability of the Physitrack® application from the players' perspective, considering aspects such as ease of use and user satisfaction.

The main questions this study aims to answer are:

Do exercise programs conducted through an online telemedicine platform achieve good adherence among handball players? Do exercise programs carried out via this telerehabilitation platform improve performance in vertical jumping? Do exercise programs performed using this platform provide good usability and user satisfaction results? To answer these questions, researchers will compare two groups following different exercise programs. The study will analyze whether, in addition to improving adherence, a specific program designed to enhance vertical jumping yields better results compared to a more general exercise program.

Participants:

Will perform a vertical jump test using force plates. Must follow the assigned eight-week exercise program according to randomization.

Will repeat the vertical jump test at the end of the program.

Enrollment

28 patients

Sex

Male

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Men over 18 years old who are part of the Móstoles Handball Club team

Exclusion criteria

  • Injured players at the start of the study and players who do not wish to participate

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

28 participants in 2 patient groups

Specific exercise program
Experimental group
Description:
8 weeks specific exercise program. Plyomteric exercises
Treatment:
Other: Specific exercise program
Control
Active Comparator group
Description:
8 weeks general exercise program
Treatment:
Other: General exercise program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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