Description Module

Description Module

The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.

Description Module path is as follows:

Study -> Protocol Section -> Description Module

Description Module


Ignite Creation Date: 2025-12-25 @ 3:01 AM
Ignite Modification Date: 2025-12-25 @ 3:01 AM
NCT ID: NCT07047833
Brief Summary: This randomized controlled trial explored the effect of plyometric training with or without hamstring strengthening in preventing anterior cruciate ligament (ACL) injuries among female amateur athletes aged 18 to 30. Sixty participants were divided equally into two groups: one received plyometric training combined with hamstring strengthening, and the other received plyometric training only. Both groups trained twice per week over a six-week period. Outcomes measured included knee strength (flexion and extension), dynamic balance (Star Excursion Test), and functional mobility (KOOS).
Detailed Description: This study examined whether combining hamstring strengthening with plyometric training provides greater benefits in preventing anterior cruciate ligament (ACL) injuries than plyometric training alone among female amateur athletes. Conducted as a randomized controlled trial, the research involved 60 participants aged 18 to 30, randomly assigned to two equal groups. Group A underwent a six-week intervention involving both plyometric and hamstring strengthening exercises, while Group B participated in plyometric training only. Each group trained twice weekly, and the outcomes were measured at baseline, Week 3, and Week 6 using a handheld dynamometer for knee strength (flexion and extension), the Star Excursion Balance Test (SET) for dynamic balance, and the Knee Injury and Osteoarthritis Outcome Score (KOOS) for functional mobility.
Study: NCT07047833
Study Brief:
Protocol Section: NCT07047833