Effects of home-based and remotely supervised exercise programs on non-motor symptoms in early Parkinson’s disease: a feasibility pilot study

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CRIS

Registry ID

KCT0008302

Enrollment

Registered

2023-03-17

Start date

2023-03-20

Completion date

Unknown

Last updated

2023-06-26

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

Conditions

None listed

Interventions

Others(Physical exercise) : Exercise Venue: Incheon University Sports Center 2nd floor (for group education only) and at home Instructor: The exercise program will be conducted by a certified health e

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Patients who were diagnosed with Parkinson's disease based on the UK Parkinson's Disease Society Brain Bank Diagnostic Criteria 2) Patients who were aged between 50 and 80 3) Patients with Hoehn and Yahr stage 1 or 2 4) Patients with the disease duration of less than 5 years 5) Patients who had a score = 1 in the MDS-UPDRS part 1 6) Patients who did less than the recommended aerobic exercise proposed by the American College of Sports Medicine (ACSM) (ex. vigorous exercise done <3 times per week, 20 min per session; or moderate exercise done <5 times per week, 30 min per session) 7) Patients who were on stable dopaminergic pharmacotherapy over more than 3 months

Exclusion criteria

Exclusion criteria: 1) Patients with neurological, orthopedic, or cardiac comorbidities that make them unfit to do exercise 2) Patients who were unable to complete questionnaires due to cognitive impairment 3) Patients on antipsychotics 4) Patients who have symptoms or signs suggesting atypical or secondary parkinsonism (ex. cerebellar signs, supranuclear gaze palsy, apraxia, prominent autonomic failure, or other cortical signs; multiple strokes with stepwise progression of symptoms) 5) Patients who were unavailable for more than 10% of the study period

Design outcomes

Primary

Measure	Time frame
Retention rate;Adherence rate;Change in scores of the Korean Dementia Rating Scale-2	—

Secondary

Measure	Time frame
Change in scores of the MDS-UPDRS part 1;Change in scores of the MDS-UPDRS part 2;Change in scores of the MDS-UPDRS part 3;Change in scores of the BDI;Change in scores of the BAI;Change in scores of the AS	—

Countries

Korea, Republic of

Contacts

Public ContactRyul Kim

Inha University Hospital

arkrk86@gmail.com+82-32-890-3764

Outcome results