- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06817538
Investigation of the Effects of Dual Task Training on Dual Task Performance in Individuals With Scoliosis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Ankara, Turkey, 06000
- Faculty of Physiotherapy and Rehabilitation, Hacettepe
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Individuals between the ages of 10-16
- Individuals with idiopathic scoliosis
- Individuals with curve degrees between 10 and 40
- Individuals with a body mass index of less than 30 kg\m2.
- Be willing to participate in the tests and have the cognitive ability to complete the tests.
Exclusion Criteria:
- Having other types of scoliosis other than idiopathic scoliosis
- Individuals with previous scoliosis or any spine-related conservative treatment or surgery
- Acute (fracture, surgery); cardiovascular system (heart failure, arrhythmia...); nervous system diseases (epilepsy, vertigo...); sensory organs (vision or hearing loss...); musculoskeletal disorders (rheumatism, hypermobility syndrome...)
- Taking any regular medication that may affect balance (ssri, psycholeptic, anti-epileptic medication...)
- Playing sports at a professional level
- Using a brace, starting to use a brace
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Single Task Group
Control
|
Arm 1: Scoliosis-Specific Exercises Combined with Dual-Task Cognitive Training Participants with idiopathic scoliosis in this group received scoliosis-specific physiotherapeutic exercises combined with dual-task cognitive training. The intervention included motor exercises performed on balance boards and stability trainers to enhance postural control. While engaging in these motor exercises, participants simultaneously performed cognitive tasks such as word recall, identifying cities or countries starting with a given letter, and other memory-based games. This dual-task approach aimed to improve both motor and cognitive functions. Arm 2: Scoliosis-Specific and Motor Exercises Only Participants with idiopathic scoliosis in this group performed scoliosis-specific physiotherapeutic exercises along with motor exercises aimed at improving postural stability. The motor exercises were conducted using balance boards and stability trainers, focusing solely on physical performance without the |
|
Other: Dual Task Group
Study
|
Arm 1: Scoliosis-Specific Exercises Combined with Dual-Task Cognitive Training Participants with idiopathic scoliosis in this group received scoliosis-specific physiotherapeutic exercises combined with dual-task cognitive training. The intervention included motor exercises performed on balance boards and stability trainers to enhance postural control. While engaging in these motor exercises, participants simultaneously performed cognitive tasks such as word recall, identifying cities or countries starting with a given letter, and other memory-based games. This dual-task approach aimed to improve both motor and cognitive functions. Arm 2: Scoliosis-Specific and Motor Exercises Only Participants with idiopathic scoliosis in this group performed scoliosis-specific physiotherapeutic exercises along with motor exercises aimed at improving postural stability. The motor exercises were conducted using balance boards and stability trainers, focusing solely on physical performance without the |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Single Motor - Cadence
Time Frame: From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week)
|
10 meter walking test.
Measurements will begin with the participant's first step from the starting line and will end as they cross the finish line.
Each participant will complete three trials, during which the step count and duration will be recorded.
Based on these evaluations cadence (steps/min) will be calculated.
|
From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week)
|
|
Single Motor - Step Lengths
Time Frame: From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week)
|
10 meter walking test.
Measurements will begin with the participant's first step from the starting line and will end as they cross the finish line.
Each participant will complete three trials, during which the step count and duration will be recorded.
Based on these evaluations step lengths (m) will be calculated.
|
From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week)
|
|
Single Motor - Walking Speed
Time Frame: From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week)
|
10 meter walking test.
Measurements will begin with the participant's first step from the starting line and will end as they cross the finish line.
Each participant will complete three trials, during which the step count and duration will be recorded.
Based on these evaluations, walking speed (m/min) will be calculated.
|
From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week)
|
|
Single Cognitive
Time Frame: From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week)
|
Stroop Test
|
From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week)
|
|
Dual-Task ( Number)
Time Frame: From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week).
|
Giving specific cognitive tasks during a 10m walk.
These cognitive tasks will be counting backwards in 7's from a random number between 50-100.
|
From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week).
|
|
Dual-Task (Letter)
Time Frame: From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week).
|
Participants will read a 5-letter word backward during a 10-meter walk.
Each word will be provided randomly, and participants will be instructed to articulate the letters of the word in reverse order while walking.
|
From baseline assessment to post-intervention at 12 weeks (after 12 exercise sessions, one session per week).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body Asymmetry and Posture Assessments
Time Frame: Baseline measurements conducted at the initial assessment. Participants will undergo a 12-week exercise intervention, with one session per week. Post-treatment assessments will be conducted immediately after completing the 12 sessions at the 12th week.
|
Anterior and Posterior Trunk Symmetry Index
|
Baseline measurements conducted at the initial assessment. Participants will undergo a 12-week exercise intervention, with one session per week. Post-treatment assessments will be conducted immediately after completing the 12 sessions at the 12th week.
|
|
Scoliosis-specific assessments 2
Time Frame: Baseline measurements conducted at the initial assessment. Participants will undergo a 12-week exercise intervention, with one session per week. Post-treatment assessments will be conducted immediately after completing the 12 sessions at the 12th week.
|
Anterior Trunk Rotation.
The ATR is measured with the help of a scoliometer (inclinometer), a scoliosis measuring device, which evaluates the rotation of the trunk in degrees with the patient in a forward-bent position (Adam's Test position)
|
Baseline measurements conducted at the initial assessment. Participants will undergo a 12-week exercise intervention, with one session per week. Post-treatment assessments will be conducted immediately after completing the 12 sessions at the 12th week.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HUTez_001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Idiopathic Scoliosis
-
National Scoliosis CenterCompletedAdolescent Idiopathic Scoliosis (AIS) | Neuromuscular Scoliosis | Juvenile Idiopathic Scoliosis | Infantile Idiopathic Scoliosis | Ealy Onset ScoliosisUnited States
-
Lahore University of Biological and Applied SciencesGhurki Trust and Teaching HospitalNot yet recruitingScoliosis Idiopathic | Idiopathic Adolescent ScoliosisPakistan
-
Uppsala UniversityUniversity of Oslo; Linkoeping University; Örebro University, Sweden; Skane University... and other collaboratorsNot yet recruitingIdiopathic Adolescent Scoliosis | Idiopathic Juvenile ScoliosisSweden
-
Hasan Kalyoncu UniversityNot yet recruitingScoliosis Idiopathic | Scoliosis Idiopathic Adolescent | Caregiver AnxietyTurkey (Türkiye)
-
Cairo UniversityRecruitingScoliosis Idiopathic | Adolescent Idiopathic ScoliosisEgypt
-
Istinye UniversityRecruitingScoliosis Idiopathic Adolescent Treatment | Scoliosis Idiopathic AdolescentTurkey (Türkiye)
-
Medtronic Spinal and BiologicsMedical Metrics Diagnostics, IncTerminatedAdolescent Idiopathic Scoliosis | Juvenile Idiopathic ScoliosisUnited States, Canada, United Kingdom
-
Spino Modulation Inc.TerminatedAdolescent Idiopathic Scoliosis | Juvenile Idiopathic ScoliosisCanada
-
EUROSRecruitingScoliosis Idiopathic | Consent Forms | Scoliosis NeuromuscularFrance
-
Dr. Casey Stondell, MDPacira Pharmaceuticals, IncCompletedAdolescent Idiopathic Scoliosis | Juvenile Idiopathic ScoliosisUnited States
Clinical Trials on Physiotherapy/Exercise Program
-
Aveiro UniversityNot yet recruitingFrailty | Sarcopenia | Ageing | Decline, Cognitive
-
Eastern Mediterranean UniversityUnknownLumbar Disc HerniationCyprus
-
Bandırma Onyedi Eylül UniversityEnrolling by invitation
-
NHS LothianCompleted
-
Aysan YaghoubiCompletedRotator Cuff TearsTurkey (Türkiye)
-
Benha UniversityRecruitingTelerehabilitation | Physiotherapy | Medial EpicondylitisEgypt
-
Poznan University of Physical EducationRecruiting
-
Istanbul Gelisim UniversityCompletedChronic Non-Specific Neck PainTurkey (Türkiye)
-
KU LeuvenFund for Scientific Research, Flanders, BelgiumCompletedCritical Illness | Muscle Weakness | Intensive Care | DeconditioningBelgium
-
Umm Al-Qura UniversityNot yet recruitingFrailty | Falls | Mobility Limitations | Balance Deficits