A Personalized Trunk Stability Exercise Program Study With Brain Disease Patients

NCT ID: NCT06274463

Last Updated: 2024-02-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-21

Study Completion Date

2024-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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Brain Diseases

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Brain disease

Group Type EXPERIMENTAL

Exercise therapy including a trunk stabilization exercise program

Intervention Type BEHAVIORAL

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

Interventions

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Exercise 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

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

19 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bundang CHA Hospital

OTHER

Sponsor Role lead

Responsible Party

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MinYoung Kim, MD, PhD

Principle investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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MinYoung Kim, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

CHA Bundang Medical Center

Central Contacts

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MinYoung Kim, MD, PhD

Role: CONTACT

82-31-780-6281

Other Identifiers

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2023-11-035

Identifier Type: -

Identifier Source: org_study_id

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