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Feasibility of Whole-body Drumming Classes for People With Parkinson's Disease

Feasibility and Effects of Whole-body Drumming Classes on Walking in People With Parkinson's Disease: a Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04982003
Enrollment
38
Registered
2021-07-29
Start date
2019-02-22
Completion date
2022-07-30
Last updated
2023-02-01

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

Conditions

Parkinson Disease

Brief summary

People with Parkinson's disease (PD) experience difficulty with gait, postural instability, and lack of movement coordination and rhythmic timing. Non-motor functions affected by PD include time perception, feelings of apathy, depression, decreased self-efficacy, and decrease self-reported quality of life. There is currently a lack of information on how a therapeutic drumming class that uses whole-body large-amplitude movements to music would impact these motor and non-motor impairments in individuals with PD. The primary purpose of this study is to assess the feasibility of a 10-week whole-body drumming class to music specifically selected for its rhythmic structure, and effects on movement rhythm and time perception in individuals with PD. The secondary purpose is to assess the effects of the drumming class on apathy, depression, self-efficacy and health-related quality of life. Participants will be included if they have a diagnosis of PD and are able to move for an hour with rests, either standing or seated. Participants are tested before and after the class series and one month following.

Interventions

OTHERexercise

10 weekly hour-long classes of drumming to music using large-amplitude, whole-body movements

Sponsors

A.T. Still University of Health Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

single group, pre- post-test design

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* diagnosed with PD * independent walking short community and household distances with or without assistive device * able to participate in a 1-hour class once a week for ten weeks

Exclusion criteria

* change of Parkinson's medication or deep brain stimulation parameters within 2 weeks prior to or during the study * inability to grasp 2-inch diameter drum sticks * any conditions with contraindications to lift upper extremities overhead * any medical restrictions to exercise

Design outcomes

Primary

MeasureTime frameDescription
Step Cadence Variabilitywithin 7 days before the interventionVariability (SD) of step cadence
Stride Length Variabilitywithin 7 days before the interventionVariability (SD) of stride length
Change in repeated finger-tappingwithin 7 days before the intervention and within 7 days after interventionchange in inter-tapping intervals (ms) change from pre- to post-intervention

Secondary

MeasureTime frameDescription
Geriatric Depression Scale (GDS)within 7 days before the intervention and within 7 days after interventionchange in depression (GDS score; 0-15, higher is worse with more depression) from pre- to post-intervention
Change in Nine-hole peg test (NHP) duration (s)within 7 days before the intervention and within 7 days after interventionchange in speed of manual dexterity (s on NHP) from pre- to post-intervention
Lille Apathy Rating Scale (LARS)within 7 days before the intervention and within 7 days after interventionchange in apathy (LARS score; -36 to +36, lower is better with less apathy) from pre- to post-intervention
General Self-Efficacy scale (GSE)within 7 days before the intervention and within 7 days after interventionchange in self-efficacy (GSE score; 10-40, higher is better with more self-efficacy) from pre- to post-intervention
Change in Physical Performance Test (PPT) scorewithin 7 days before the intervention and within 7 days after interventionchange in whole-body functional mobility (PPT score; 0-36; higher is better) from pre- to post-intervention.
Change in Parkinson Disease Questionnaire (PDQ-39)within 7 days before the intervention and within 7 days after interventionchange in disease-related quality of life (PDQ-39 score; 0-100, lower is better with improved quality of life) from pre- to post-intervention

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026