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Parkinsonics: A Controlled Study of Group Singing in Parkinson Disease

Parkinsonics: A Controlled Study of Group Singing for Quality of Life and Voice Outcomes in Parkinson Disease

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02753621
Acronym
Parkinsonics
Enrollment
32
Registered
2016-04-28
Start date
2015-12-01
Completion date
2016-12-31
Last updated
2017-03-01

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

Conditions

Parkinson Disease

Brief summary

The overall objective of this study is to observe the effect of group Vocal performance training and performance experience on patients' reported symptoms and quality of life. The effectiveness of PD medications varies significantly in different patients depending on their symptoms. By using music-based interventions to improve symptoms that may be inadequately treated by medications, the investigators hope to improve quality of life in PD patients. Parkinsonics: A controlled study of group singing for quality of life and voice outcomes in Parkinson disease (PD) is a controlled crossover behavioral intervention study of once weekly choral classes for patients with idiopathic PD (progressing toward a group performance) and once weekly discussion/support group meetings.

Interventions

BEHAVIORALGroup singing

Weekly group singing classes led by professional choir instructor, lasting 90 minutes. 12 classes over 12 consecutive weeks.

BEHAVIORALFacilitated Discussion Group

Weekly facilitated discussion group led by Parkinson Disease educator, lasting 90 minutes. 12 sessions over 12 consecutive weeks.

Sponsors

Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 89 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of idiopathic PD based on UK Parkinson's Disease Society Brain Bank Clinical Diagnostic Criteria for PD (Hughes et al. 1992).

Exclusion criteria

* Patients unable to consent to the study. * Patients unable or unwilling to participate in weekly singing classes for 12 weeks, or unwilling to perform in a concert setting. * Patients with active psychiatric disturbances (agitation, active hallucinations).

Design outcomes

Primary

MeasureTime frameDescription
Parkinson Disease Quality of Life Questionnaire (PDQ)-39 scoresChange from baseline scores at 30 weeksValidated 39-item questionnaire

Secondary

MeasureTime frameDescription
Geriatric Depression Scale-15Change from baseline scores at 30 weeksValidated depression self-rating
Lorig Self-efficacy scaleChange from baseline scores at 30 weeks5-item self-reported questionnaire
Short Form-36Change from baseline scores at 30 weeksSelf-reported questionnaire assessing patients' health based on their physical and mental well-being
Voice-Related Quality of LifeChange from baseline scores at 30 weeksValidated 10-item questionnaire
Movement Disorder Society-Unified Parkinson Disease Rating Scale Motor scoresChange from baseline scores at 30 weeksValidated Parkinson disease motor assessment scale
Sound pressure level (decibels)Change from baseline levels at 30 weeksAssessed while reading the standardized Rainbow passage and describing the cookie theft picture at a 50cm distance from the microphone (using a portable professional decibel meter).
Voice jitterChange from baseline values at 30 weeksAnalysis will be performed using Praat software (Boersma and Weenink, version 5.4.01, http://www.fon.hum.uva.nl/praat/). There will be 3 trials per subject holding sounds A and E for as long as possible on one breath. Sound recordings are made for each trial.
Voice shimmerChange from baseline values at 30 weeksAnalysis will be performed using Praat software (Boersma and Weenink, version 5.4.01, http://www.fon.hum.uva.nl/praat/). There will be 3 trials per subject holding sounds A and E for as long as possible on one breath. Sound recordings are made for each trial.
Harmonic to noise ratioChange from baseline values at 30 weeksAnalysis will be performed using Praat software (Boersma and Weenink, version 5.4.01, http://www.fon.hum.uva.nl/praat/). There will be 3 trials per subject holding sounds A and E for as long as possible on one breath. Sound recordings are made for each trial.
Montreal Cognitive AssessmentChange from baseline scores at 30 weeksValidated cognitive assessment

Other

MeasureTime frameDescription
Feasibility12 weeksAt least 80% of participants attending at least 9 of 12 singing classes and the final performance

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026