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Effect of neuromuscular training on improving medial tibial stress syndrome

Neuromuscular training program for treatment of male basketball players with medial tibial stress syndrome: emphasis on attentional focus and external cues in functional movement training.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210718051938N1
Enrollment
72
Registered
2021-08-01
Start date
2021-08-09
Completion date
Unknown
Last updated
2023-05-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Medial tibial stress syndrome. Other injury of other muscles and tendons at lower leg level

Interventions

Intervention 1: First intervention group: Benjaminse et al. (2015) training protocol will be used for the first intervention group. These exercises include eight different types of exercises, in each

Sponsors

Kharazmi University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Male basketball players between 18 and 35 years ages For at least 3 weeks’ exercise, induced pain located on the posteromedial border of the tibia, palpation of the posteromedial border of the tibia that produces discomfort, will be diagnosed by experienced sports medicine.

Exclusion criteria

Exclusion criteria: Having a history of tibial fracture Clinical suspicion of chronic compartment syndrome or stress fracture

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Baseline, 6 weeks after intervention, 3, 6, and 12 months follow up. Method of measurement: How to measure a variable is using Visual Analogue Scale.

Secondary

MeasureTime frame
Function. Timepoint: Baseline, 6 weeks after intervention, 3, 6, and 12 months follow up. Method of measurement: How to measure a variable is using vertical jump.;Muscle strength. Timepoint: Baseline, 6 weeks after intervention, 3, 6, and 12 months follow up. Method of measurement: How to measure a variable is using Biodex System isokinetic.;Kinematic. Timepoint: Baseline, 6 weeks after intervention, 3, 6, and 12 months follow up. Method of measurement: How to measure a variable is using Visual3D software (C-motion Inc, Germantown).;Kinetic, Tibia acceleration and Time to Stabilization. Timepoint: Baseline, 6 weeks after intervention, 3, 6, and 12 months follow up. Method of measurement: How to measure a variable is using Two three-axis force plates (AMTI model) in vertical, anterior-posterior, and medial-lateral.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Letafatkar

Kharazmi Univesity

letafatkaramir@yahoo.com+98 21 2222 1008

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026