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A Personalized Trunk Stability Exercise Program Study With Brain Disease Patients

Effects of Customized Trunk Stabilization Exercise Program to Patients With Brain Disease on Trunk Stability and Satisfaction With the Program

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06274463
Enrollment
10
Registered
2024-02-23
Start date
2024-02-21
Completion date
2024-12-31
Last updated
2024-02-23

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

Conditions

Brain Diseases

Brief summary

To investigate the effect on improving trunk stability and satisfaction with the program when a customized trunk stabilization exercise program personalized to the subject's functional level is applied to patients with brain disease.

Interventions

BEHAVIORALExercise therapy including a trunk stabilization exercise program

All patients will undergo 30 sessions of exercise therapy, including a trunk stability exercise program, for 30 minutes per day, 5 days a week for 6 weeks

Sponsors

Bundang CHA Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Adults over 19 years old 2. Brain disease patients hospitalized in the rehabilitation medicine department of our hospital and receiving exercise therapy 5 times a week 3. Patients with a functional ambulatory category (FAC) score of 0-4 4. After receiving a detailed explanation of this study and fully understanding it, the subject or legal representative voluntarily decides to participate and agrees in writing to follow the precautions.

Exclusion criteria

1. Those who have suffered prior to participating in the study 2. Those in good physical condition, such as unstable conditions in the state system, coordination system, problem system, and endocrine system, and those with cerebrovascular disease 3. Other cases of investigation without participation in this study

Design outcomes

Primary

MeasureTime frameDescription
Trunk Impairment Scalebaseline, 5 weeks after interventionTrunk impairment scale assessment for motor function of upper extremity in score. This evaluation consists of a total score of 23 points and consists of static sitting balance, dynamic sitting balance, and co-ordination. The higher the score, the better the upper extremity motor function.
Berg Balance Scalebaseline, 5 weeks after interventionBerg balance scale assessment of balance function by score. It consists of a total of 14 items and is divided into three parts: sitting, standing, and posture change. The minimum score is 0 points, up to 4 points for discharge, and the total total score is 56 points. A higher score means higher balance ability and lower risk of falling.

Secondary

MeasureTime frameDescription
Joint momentbaseline, 5 weeks after interventionEvaluating kinetic parameters of joint moment (Nm/kg) of each joint through Qualisys motion analysis system.
Joint anglebaseline, 5 weeks after interventionMotion analysis is a process of measuring and evaluating kinematic parameters of joint angle(degree) of each joint through Qualisys motion analysis system.
Joint powerbaseline, 5 weeks after interventionEvaluating kinetic parameters of joint power(Nm/s\*Kg) of each joint through Qualisys motion analysis system.

Contacts

Primary ContactMinYoung Kim, MD, PhD
kmin@cha.ac.kr82-31-780-6281

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026