Home-based Self-exercise in Patients With Parkinson's Disease: A Feasibility Study
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19+
SponsorSeoul National University Hospital
About this trial
This study aims to test whether patients with Parkinson's disease can safely and effectively use a home-based exercise program guided by videos. Participants will follow video instructions for exercises at home while their movements are monitored by a camera, which provides real-time feedback. The study will check how well participants complete the exercises, their satisfaction with the program, and any changes in clinical function. The goal is to see if this type of home exercise can help patients increase their activity levels without significant side effects.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults aged 19 years or older, clinically diagnosed with Idiopathic Parkinson's Disease (PD) according to the Movement Disorder Society (MDS) clinical diagnostic criteria
Patients at Hoehn and Yahr stage 1-2.5
Patients on stable dopaminergic therapy with no changes in the past 1 month
Patients receiving Lee Silverman Voice Treatment (LSVT) rehabilitation therapy once weekly as outpatients
Disqualifiers
Patients diagnosed with atypical parkinsonism
Patients with musculoskeletal problems that make participation in rehabilitation difficult
Patients who have limited access to the video-based home exercise feedback program
Trial design
Design model
Single group
Treatments tested in this trial
Home-based self-exercise feedback program using video
BehavioralParticipants follow a 6-week home-based exercise program using video-guided instructions and the iPixel exercise feedback system, which monitors movements in real-time and provides corrective feedback. The program includes: Stretching exercises, Strength training, Balance exercises, Aerobic exercises, LSVT-specific exercises. Participants are instructed to complete sessions at least 5 times per week, 40 minutes per session. Additionally, weekly 30-minute in-person rehabilitation sessions are conducted to adjust the next week's exercise intensity based on each participant's functional level.
Treatment groups
15 Participants
are divided into 1 treatment groupGroup A: Home-based Exercise Program (Single Arm)Experimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS), Part III (Motor Examination)
0 to 108, with higher scores indicating worse motor function.
Time frame
From enrollment to the end of treatment at 6 weeksSecondary outcomes
1
Modified Hoehn and Yahr sacle
Modified Hoehn and Yahr Scale Score range: 0 to 5, with higher scores indicating more severe disease stage.
Time frame
From enrollment to the end of treatment at 6 weeks2
Berg Balance Scale
0 to 56, with higher scores indicating better balance ability.
Time frame
From enrollment to the end of treatment at 6 weeks3
Functional Gait Ability
0 to 30, with higher scores indicating better gait function.
Time frame
From enrollment to the end of treatment at 6 weeks4
Freezing of Gait Questionnaire
0 to 24, with higher scores indicating more severe freezing of gait.
Time frame
From enrollment to the end of treatment at 6 weeksSponsors and contacts
Click on the lead sponsor to view all of their trials.
Seoul National University Hospital
Lead sponsor
Seoul National University Bundang Hospital
Sponsor institution
Source ClinicalTrials.gov
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