The Effect of Combined Speech and Music-therapy on the Speech Characteristics of People With Parkinson's Disease (PD)

Sponsor
Iran University of Medical Sciences (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04966689
Collaborator
(none)
33
3
14.8

Study Details

Study Description

Brief Summary

Speech and voice disorders are observed in almost 90% of patients with PD during their course of illness. Reduced voice pitch inflections or monotone speech, reduced vocal loudness, prosody disorders, the imprecise articulation of the consonants, hoarseness, and breathy voice is also observed in patients with PD; these symptoms often lead to reduced speech intelligibility. The aim of this study will to investigate the possible changes in the voice and speech features in people with PD after a combined speech and music therapy using Telerehabilitation.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: combined speech and music therapy
  • Behavioral: speech therapy
  • Behavioral: music therapy
N/A

Detailed Description

the investigators of this study propose to conduct a pilot randomized, controlled trial in patients with PD to assess the potential effectiveness of a Telerehabilitation intervention that encourage a higher level of speech performance. The investigators hypothesize that patients in the combined treatment group will have more and better improve in the study outcome measures after treatment and 3 month follow up, as compared with patients in speech therapy group and music therapy group.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
33 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Comparison of The Effect of Speech Therapy , Music-therapy and Combined Speech and Music Therapy on the Vocal Characteristics of People With PD by Using Telerehabilitation
Anticipated Study Start Date :
Aug 7, 2022
Anticipated Primary Completion Date :
Jan 7, 2023
Anticipated Study Completion Date :
Oct 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: combined speech and music therapy

the telerehabilitation intervention that include both speech therapy and music therapy at the same time

Behavioral: combined speech and music therapy
he telerehabilitation intervention that include both speech therapy and music therapy at the same time

Active Comparator: speech therapy

A behavioural speech therapy program including breathing exercises, loudness, pitch, and intelligibility which are adapted from Lee Silverman Voice Treatment (LSVT) and voice exercises Which is delivered through telerehabilitation

Behavioral: speech therapy
A behavioural speech therapy program including breathing exercises, loudness, pitch, and intelligibility which are adapted from Lee Silverman Voice Treatment (LSVT) and voice exercises Which is delivered through telerehabilitation

Active Comparator: music therapy

music exercises Will be designed based on the music therapy protocols of previous studies Which is delivered through telerehabilitation

Behavioral: music therapy
music exercises Will be designed based on the music therapy protocols of previous studies Which is delivered through telerehabilitation

Outcome Measures

Primary Outcome Measures

  1. loudness [Change from Baseline in loudness at 4 weeks and 3 month follow up]

    Change in loudness over the period of the study which will be based on analysis of acoustic recordings. Loudness of voice will be measured in produce the vowel /a /, reading and spontaneous speech. Data will be analyzed using Praat, freeware program for the analysis and reconstruction of acoustic speech signals.

Secondary Outcome Measures

  1. Voice Handicap Index (VHI) [Change from Baseline in VHI at 4 weeks and 3 month follow up]

    Change in Persian version of Voice Handicap Index (VHI) over the period of the study. The VHI measures the influence of voice problems on a patient's quality of life. The VHI is a 30 item scale. The total scores range is 0-120. A score 60-120 indicates severe voice problem.

  2. maximum phonation time (MPT) [Change from Baseline in MPT at 4 weeks and 3 month follow up]

    Change in maximum phonation time (MPT) over the period of the study. MPT will be measured by asking the subject to produce the long vowel /a/. This vocalization is measured three times, and the longest MPT is recorded.

  3. Speech Intelligibility [Change from Baseline in Speech Intelligibility at 4 weeks and 3 month follow up]

    Change in fudalla speech intelligibility rating scale over the period of the study. This scale consists of 7 rates in which the number 1 indicates Speech is not intelligible and number 7 indicates Speech is totally intelligible.

  4. Swallowing Disturbance Questionnaire (SDQ) [Change from Baseline in SDQ at 4 weeks and 3 month follow up]

    Change in Persian version of Swallowing Disturbance Questionnaire (SDQ) over the period of the study. The SDQ is a 15 item scale. The total scores range is 0-45. A score higher 11 indicates swallowing difficulty.

  5. Dysphagia handicap index (DHI) [Change from Baseline in DHI at 4 weeks and 3 month follow up]

    Change in Persian version of Dysphagia handicap index (DHI) over the period of the study. The DHI is one of the instruments used for measuring a dysphagic patient's self-assessment. it reflects the patient's quality of life. DHI is a 25 item scale. The total scores range is 0-100. A higher score indicates a greater impact of swallowing disorders on quality of life

  6. northwest dysphagia patient check sheet (NDPCS) [Change from Baseline in NDPCS at 4 weeks and 3 month follow up]

    Change in Persian version of northwest dysphagia patient check sheet (NPCS) scores over the period of the study. The NDPCS has five and 28 items. Each item is scored as safe or unsafe. The total score is calculated from the total number of unsafe items. The more unsafe observations indicates swallowing difficulty.

  7. Geriatric Depressive Scale (GDS) [Change from Baseline in GDS at 4 weeks and 3 month follow up]

    Change in Persian version of Geriatric Depressive Scale (GDS) scores over the period of the study. GDS is a 15 item scale. Each item is scored as yes or no. More than 5 signs indicate the possibility of depression and more than 10 signs of depression indicate definite depression.

  8. quality of life (QoL) [Change from Baseline in QOL at 4 weeks and 3 month follow up]

    Change in SF-36 questionnaire over the period of the study. Quality of life will be measured using SF-36 questionnaire. SF-36 is a 36 item scale. The total scores range is 0-100. A higher score indicates a better quality of life.

  9. jitter [Change from Baseline in jitter at 4 weeks and 3 month follow up]

    Change in jitter over the period of the study, which will be based on analysis of acoustic recordings. jitter will be measured in produce the vowel /a/. Data will be analyzed using Praat, freeware program for the analysis and reconstruction of acoustic speech signals.

  10. shimmer [Change from Baseline in shimmer at 4 weeks and 3 month follow up]

    Change in shimmer over the period of the study, which will be based on analysis of acoustic recordings. shimmer will be measured in produce the vowel /a/. Data will be analyzed using Praat, freeware program for the analysis and reconstruction of acoustic speech signals.

  11. highest and lowest frequency [Change from highest and lowest frequency at 4 weeks and 3 month follow up]

    Change in highest and lowest frequency over the period of the study, which will be based on analysis of acoustic recordings. highest and lowest frequency will be measured by asking the subject to produce the vowel /a/ as high and low frequency as they can produces. Data will be analyzed using Praat, freeware program for the analysis and reconstruction of acoustic speech signals.

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients with idiopathic Parkinson's disease (IPD)

  • Patients who are in stages 1-3 according to Hoehn & Yahr test

  • Native language is persian

  • The patient or family complains about the person's speech condition

  • Adequate vision and hearing

  • No history of stroke, head injury, brain surgery, laryngeal diseases such as vocal cord nodules

  • No other neurological disorders other than IPD

  • Do not use treatment other than medication (such as deep brain stimulation surgery (DBS)

  • informed consent

Exclusion Criteria:
  • If a patient develops a stroke or other neurological complication during treatment, they are excluded from the treatment

  • Lack of cooperation

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Iran University of Medical Sciences

Investigators

  • Study Director: Reyhaneh Mohammadi, Iran university of medical science

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Iran University of Medical Sciences
ClinicalTrials.gov Identifier:
NCT04966689
Other Study ID Numbers:
  • 1
First Posted:
Jul 19, 2021
Last Update Posted:
Jan 11, 2022
Last Verified:
Jun 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 11, 2022