Effects of Motor Imagery on Autonomic Function
1 other identifier
interventional
54
1 country
1
Brief Summary
Most studies on motor imagery suggested the effects of motor imagery are related to neuroplastic changes in the brain. In addition to that the neuroplastic changes, it is thought that motor imagery can alter metabolic responses just like in actual exercise. However, the level of evidence about the effect of motor imagery on autonomic functions is limited. The aims of this study;
- 1.The primary aim of this study is to investigate the effects of activating and relaxing kinesthetic motor imagery on autonomic function in healthy individuals and to compare these two methods.
- 2.The secondary aim of this study is to explore the effects of these methods on motor imagery skills of individuals will also be investigated.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2019
Shorter than P25 for not_applicable
1 active site
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
First Submitted
Initial submission to the registry
November 18, 2019
CompletedFirst Posted
Study publicly available on registry
November 20, 2019
CompletedStudy Start
First participant enrolled
November 21, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 31, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2020
CompletedFebruary 17, 2021
February 1, 2021
4 months
November 18, 2019
February 16, 2021
Conditions
Outcome Measures
Primary Outcomes (4)
Feasibility of the methods - minimum recruitment rate
A minimum recruitment rate of 10 participants per month will be accepted as feasiable.
through Study Completion, an Average of 8 Months
Feasibility of the methods - minimum retention rate
A target retention rate of 80% will be accepted as feasiable.
through Study Completion, an Average of 8 Months
Feasibility of the methods - minimum adherence rate
A target minimum adherence rate of 70% of the overall practice sessions will be accepted as feasiable.
through Study Completion, an Average of 8 Months
Feasibility of the methods - adverse events
A record sheet was prepared for possible adverse events during the tests and intervention. It includes information about seriousness, expectedness, severity, causality, time, duration of the event and clinical action taken. The numbers of adverse events will be reported.
through Study Completion, an Average of 8 Months
Secondary Outcomes (7)
Edinburgh Handedness Inventory
at Baseline
Movement Imagery Questionnaire-Revised
Change from Baseline at 2 Weeks
Mental chronometry for walking task
Change from Baseline at 2 Weeks
Mental chronometry for writing task
Change from Baseline at 2 Weeks
Hand Laterality Judgement Measurement
Change from Baseline at 2 Weeks
- +2 more secondary outcomes
Study Arms (3)
Activating kinesthetic motor imagery training
EXPERIMENTALRelaxing kinesthetic motor imagery training
ACTIVE COMPARATORControl (no specific intervention)
NO INTERVENTIONInterventions
Participants in the activating kinesthetic motor imagery training group will imagine high effort exercises (e.g. planking, boxing, jumping, squats, push-ups) in the sessions in home using the study audio-video motor imagery script for 5 times per week; 17 min per day for 2 weeks. Phone calls will be performed for support and as a reminder for the assessment (after one week).
Participants in the relaxing kinesthetic motor imagery training group will imagine relaxing (low effort) exercises (e.g. breathing exercises, stretching, body awareness exercises) in home using the study audio-video motor imagery script 5 times per week; 17 min per day for 2 weeks. Phone calls will be performed for support and as a reminder for the assessment (after one week).
Eligibility Criteria
You may qualify if:
- Being healthy (not having any known chronic disease)
- Volunteer to participate in the study
You may not qualify if:
- Pregnancy
- Previous disorder/surgery history that can alter physical performance
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Izmir Katip Celebi University
Izmir, 35620, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
November 18, 2019
First Posted
November 20, 2019
Study Start
November 21, 2019
Primary Completion
March 31, 2020
Study Completion
March 31, 2020
Last Updated
February 17, 2021
Record last verified: 2021-02