NCT05886062

Brief Summary

The aim of this study is to examine the investigation of the effects of motor imagery to facilitate sensorimotor re-learning training on performance and heart rate variability in adolescent basketball players.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2023

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2023

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

May 23, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

June 2, 2023

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2023

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2024

Completed
Last Updated

February 20, 2024

Status Verified

May 1, 2023

Enrollment Period

11 months

First QC Date

May 23, 2023

Last Update Submit

February 16, 2024

Conditions

Keywords

ImageryExerciseAdolescent Basketball Players

Outcome Measures

Primary Outcomes (1)

  • Balance

    The balance of the athletes will be evaluated with the Y balance test.

    change from baseline at 8 weeks

Secondary Outcomes (5)

  • Muscle Power

    change from baseline at 8 weeks

  • Muscle Strength

    change from baseline at 8 weeks

  • Shooting Performance

    change from baseline at 8 weeks

  • Agility

    change from baseline at 8 weeks

  • Heart Rate Variability

    change from baseline at 8 weeks

Study Arms (2)

Experimental Group

EXPERIMENTAL

In addition to routine basketball technical-tactical training, the athletes in the experimental group will be given motor imagery training to facilitate sensorimotor relearning.

Other: Motor Imagery to Facilitate Sensorimotor Re-Learning Training

Control Group

ACTIVE COMPARATOR

Individuals in the control group will only continue their routine basketball technical-tactical training.

Other: Control Group

Interventions

In order to motor imagery to facilitate sensorimotor re-learning training will be given for 20 minutes a day, 3 days a week, for a total of 8 weeks. Basketball-specific movement patterns will be used (squat, single leg jump, side stepping, standing on one leg, squat on one leg, etc.). Exercises will be started from easy and progressed to more advanced levels. During the exercise, the person will not only be physically active, but will be asked to dynamically visualize the determined scenario. Thus, a holistic exercise program will be applied both physically and psychologically.

Experimental Group

They will only continue their routine basketball technical-tactical training.

Control Group

Eligibility Criteria

Age11 Years - 19 Years
Sexmale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Being between the ages of 11-19
  • Playing licensed basketball for at least 2 years
  • Being a man

You may not qualify if:

  • Coming to the hospital with a musculoskeletal injury in the last 3 months
  • Not being willing to participate in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ege University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation

Izmir, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Motor Activity

Interventions

Control Groups

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Central Study Contacts

Emre Uysal, M. Sc.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

May 23, 2023

First Posted

June 2, 2023

Study Start

January 1, 2023

Primary Completion

December 1, 2023

Study Completion

August 1, 2024

Last Updated

February 20, 2024

Record last verified: 2023-05

Locations