rTMS Improves Functions in Spinocerebellar Ataxia

Sponsor
Changhua Christian Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05973019
Collaborator
(none)
10
1
12

Study Details

Study Description

Brief Summary

Spinocerebellar ataxia (SCA) is a group of inherited brain disorders. SCA often result in poor limb coordination. This study aims to discover the effects of repeated transcranial magnetic stimulation (rTMS) on balance & gait in SCA. The hypothesis of this study is that rTMS might improve SCA limb functional performance.

Condition or Disease Intervention/Treatment Phase
  • Device: Repetitive Transcranial Magnetic Stimulation (rTMS)
N/A

Detailed Description

rTMS has been shown that improves walking speed and balance performance, however, the optimal treatment protocols have not been approved. Past studies used different frequencies 1 Hz, 5 Hz and 10 Hz to improve functional performance. The results might be affected by the types of SCA. In this study, we will focus on the SCA type 3 to assess the effects on high frequency (10 Hz) of rTMS intervention.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
All subjects receive 12 times rTMS interventionAll subjects receive 12 times rTMS intervention
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Repetitive Transcranial Magnetic Stimulation Improves Functional Performance in Spinocerebellar Ataxia
Anticipated Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Jun 30, 2024
Anticipated Study Completion Date :
Aug 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: rTMS with 10 Hz

6 times/per week for 2 weeks, total 12 times rTMS.

Device: Repetitive Transcranial Magnetic Stimulation (rTMS)
6 times/per week for 2 weeks, total 12 times rTMS with 10 Hz.

Outcome Measures

Primary Outcome Measures

  1. Changes of International Cooperative Ataxia Rating Scale [Baseline (T0), 6 days after first rTMS intervention (T1), 12 days after first rTMS intervention (T2),]

    International Cooperative Ataxia Rating Scale (ICARS): quantify the level of impairment as a result of ataxia as related to hereditary ataxias. Disorders rated as subscales within the ICARS are: Postural and gait disturbances, Limb Ataxia, Dysarthria, and Oculomotor disorders.It translates the symptomatology of cerebellar ataxia into a scoring system out of 100.

  2. Changes of SARA [Baseline (T0), 6 days after first rTMS intervention (T1), 12 days after first rTMS intervention (T2),]

    Scale for the Assessment and Rating of Ataxia (SARA): a tool for assessing ataxia. It has eight categories with accumulative score ranging from 0 (no ataxia) to 40 (most severe ataxia).

  3. Changes of Berg Balance Scale [Baseline (T0), 6 days after first rTMS intervention (T1), 12 days after first rTMS intervention (T2),]

    Berg Balance Scale (BBS): a widely used assessment to determine a person's balance abilities. The test contains 14 simple tasks, scoring ranges from 0 to 56. The lower your score, the more at risk you are for losing your balance. The entire process takes about 20 minutes to complete.

  4. Changes of Timed up and go [Baseline (T0), 6 days after first rTMS intervention (T1), 12 days after first rTMS intervention (T2),]

    Timed up and go (TUG): Patients wear their regular footwear and can use a walking aid, if needed. Begin by having the patient sit back in a standard arm chair and identify a line 3 meters, or 10 feet away, on the floor.

  5. Changes of Center of pressure trajectory [Baseline (T0), 6 days after first rTMS intervention (T1), 12 days after first rTMS intervention (T2),]

    Center of pressure (COP): he trajectory of the COP, commonly known as a stabilogram, during static balance is frequently used to measure postural control. When standing still on a force platform, the COP is thought to be an indicator of the motor mechanisms involved in maintaining balance with opened-eyes or closed-eyes. Two trials for each condition were performed within 5 minutes.

  6. Changes of Kinematic of Gait [Baseline (T0), 6 days after first rTMS intervention (T1), 12 days after first rTMS intervention (T2),]

    The joint angles of hip, knee, ankle are collected during walking in a 10 meters walkway.

  7. Changes of Electromyography of Gait [Baseline (T0), 6 days after first rTMS intervention (T1), 12 days after first rTMS intervention (T2),]

    A wireless surface Electromyography (EMG) is used to collect lower extremities muscle activation signals during walking in a walkway.

Secondary Outcome Measures

  1. Concentration of Neurofilament [Baseline (T0), 12 days after first rTMS intervention (T2)]

    neurofilament proteins is the biomarkers of axonal damage in diseases affecting the central nervous system

  2. Changes of Mini-mental state examination [Baseline (T0)]

    The mini-mental state examination (MMSE) is a 30-point questionnaire that is used extensively in clinical and research settings to measure cognitive impairment. A score of 25 or higher is classed as normal. If the score is below 24, the result is usually considered to be abnormal, indicating possible cognitive impairment. In this study, it is used to rule out subjects who might have dementia.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • SCA type 3

  • independently walk with/without an assistive device

  • SARA greater than 3

Exclusion Criteria:
  • Epilepsy history

  • Unstable blood pressure

  • Brain Trauma

  • Alcoholism, drug abuse, antipsychotics drug use

  • Metallic hardware (e.g. - cochlear implants, brain stimulators or electrodes, aneurysm clips) anywhere in head.

  • Dementia, depression

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Changhua Christian Hospital

Investigators

  • Principal Investigator: Sen Yung Liu, MD, Changhua Christian Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sen-yung Liu, Chief Medical Officer, Changhua Christian Hospital
ClinicalTrials.gov Identifier:
NCT05973019
Other Study ID Numbers:
  • 230425
First Posted:
Aug 2, 2023
Last Update Posted:
Aug 4, 2023
Last Verified:
Aug 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sen-yung Liu, Chief Medical Officer, Changhua Christian Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 4, 2023