Advanced Parkinson's With Dysphagia
Conditions
Brief summary
This study aims to assess the therapeutic role of rTMS on parkinson's patients with dysphagia. Thirty PD patients with dysphagia using UK bank criteria for PD will recruited from outpatient clinic in Assuit University. All patients were admitted at Neuropsychiatric Department, Assiut University Hospital/ Assiut, Egypt. Each patient fulfilled the inclusion criteria as spontaneous swallows should be identified clearly when patients cannot perform voluntary swallows using clinical examination test. The patients will be allocated randomly into two groups one of which will receive real sessions of high frequency rTMS (25 HZ), with intensity of 80% of resting motor threshold detected from the hand motor area, with total 2000 pulses for each hemisphere for 10 consecutive sessions totally over period of 10 days with repeated booster session every month during the period of follow up among three months. The other will receive sham sessions. All subjects will be followed up by selected clinical rating scales at different intervals pre session, post 10 sessions, and after one, two and three months.
Detailed description
This study aims to assess the therapeutic role of repetitive transcranial magnetic (rTMS) on parkinson's patients with dysphagia. Thirty PD patients with dysphagia using UK bank criteria for PD will recruited from outpatient clinic in Assuit University. All patients were admitted at, Neuropsychiatric Department, Assiut University Hospital/ Assiut, Egypt. Each patient fulfilled the inclusion criteria as spontaneous swallows should be identified clearly when patients cannot perform voluntary swallows using clinical examination test. The patients will be allocated randomly into two groups using closed envelops one of which will receive real sessions of high frequency rTMS (25 HZ), with intensity of 80% of resting motor threshold detected from the hand motor area, with total 2000 pulses for each hemisphere for 10 consecutive sessions totally over period of 10 days with repeated booster session every month during the period of follow up among three months. the other will receive sham sessions. All subjects after receiving the rTMS will be followed up by selected clinical rating scales at different intervals Pre session, post 10 sessions, after one, two and three months.
Interventions
PROCEDURErepetitive transcranial magnetic (rTMS)
Real rTMS high frequency stimulation (25 HZ), with intensity of 80% of resting motor threshold detected from the hand motor area, with total 2000 pulses for each hemisphere for 10 consecutive sessions totally over period of 10 days. Sham rTMS is the same pulse as the first group but with the coil placed perpendicular to the scalp.
Sponsors
Assiut University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* All parkinson's disease patients who were diagnosed according to UK bank criteria for PD, Aged 50-75 years, with dysphagia
Exclusion criteria
* History of repeated head injury * History of repeated cerebrovascular strokes * History of defined encephalitis * Oculogyric crisis, supranuclear gaze palsy * Family history of more than one relative * History of drug intake as antipsychotics or MPTP exposure * Severe dementia, (MMSE \< 23), Severe depression (H- D) \< severe dysautonomia * Cerebellar signs * Babiniski sign * Strictly unilateral features after 3 years * Hydrocephalus or intracranial lesion on neuroimaging * We also excluded patients with intracranial metallic devices or with pacemakers or any other device. * Patients who were unable to give informed Consent because of severe anesthesia or cognitive deficit were not included.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| changes in dysphagia severity measurement | Three months | Dysphagia severity changes measured by Dysphagia Handicap Index (DHI) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| swallowing changes pre and post 10 sessions using | ten days | Measurement of swallowing changes pre and post 10 sessions using video fluoroscopy (VFS). |
Countries
Egypt
Outcome results
None listed