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PERsonalized SPEeCh Therapy for actIVE Conversation (PERSPECTIVE)

Primary Purpose

Parkinson Disease

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Speech therapy
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson Disease focused on measuring Speech therapy, Telerehabilitation, Quality of life

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • A diagnosis of idiopathic PD;
  • Problems in intelligibility affecting daily communication (as indicated by the patient and/or the caregiver);
  • A desire for improvement;
  • willing and able to receive online treatment

Exclusion Criteria:

  • Recent (<1 year) speech therapy;
  • Voice or speech problems due to other causes;
  • Communication difficulties based on language problems without predominantly reduced intelligibility;
  • inability to receive online treatment

Sites / Locations

  • Radboud university medical center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention group

Control group

Arm Description

Speech therapy, right after T0 (baseline measurement).

Patients will be on a waiting list for 8 weeks. After the primary endpoint (T1), patients will receive speech therapy.

Outcomes

Primary Outcome Measures

Disease-specific health-related quality of life
Parkinson's Disease Questionnaire (PDQ-39)

Secondary Outcome Measures

Speech quality
Radboud Dysarthria Assessment (RDA)
Voice quality
Acoustic Voice Quality Index (AVQI)
Voice handicap
Voice Handicap Index (VHI)
Severity of voice and speech complaints, reported by patient
Radboud Oral Motor inventory for Parkinson's disease (ROMP)
Severity of voice and speech complaints, reported by caregiver
Radboud Oral Motor inventory for Parkinson's disease (ROMP), adapted to caregiver
Speech intelligibility
Dutch intelligibility test - sentence level (NSVO-Z)
Caregiver burden
Zarit caregiver Burden Interview Short Form (ZBI-12)
Mood and anxiety
Hospital Anxiety and Depression Scale (HADS)
Health-related quality of life
EuroQol-5D (EQ-5D)
Swallowing
Maximum swallowing speed (timed test)

Full Information

First Posted
May 9, 2019
Last Updated
May 26, 2023
Sponsor
Radboud University Medical Center
Collaborators
Michael J. Fox Foundation for Parkinson's Research
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1. Study Identification

Unique Protocol Identification Number
NCT03963388
Brief Title
PERsonalized SPEeCh Therapy for actIVE Conversation
Acronym
PERSPECTIVE
Official Title
The PERSPECTIVE Study: PERsonalized SPEeCh Therapy for actIVE Conversation
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
March 1, 2019 (Actual)
Primary Completion Date
November 10, 2021 (Actual)
Study Completion Date
November 10, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
Collaborators
Michael J. Fox Foundation for Parkinson's Research

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Up to 70% of the patients with Parkinson's Disease (PD) experience speech problems, which cause a diminished intelligibility. A reduced intelligibility has a profound negative impact on social interaction and quality of life. Since pharmacological treatment only has limited effects on speech, non-pharmacological treatment, like speech therapy, is particularly relevant. Cochrane reviews (Herd et al., 2012a; Herd et al., 2012b) showed that evidence for speech therapy in PD is increasing, but is still inconclusive. Moreover, only very intensive standardized treatment programs have been studied, which are only feasible for people with mild to moderate PD, but too intensive for people with advanced PD. Here, the investigators will perform the first large-scale study to demonstrate the efficacy of speech therapy in PD patients in all disease stages on quality of life and speech quality. Objective: The aim is to demonstrate the effectiveness of personalized and home-based speech therapy on quality of life, intelligibility and social participation for people with Parkinson's disease who have a reduced intelligibility of speech. Methods: The investigators will perform a single blind, randomized and controlled trial. A total of 215 patients (18 years and older) with PD in all disease stages who have difficulty with intelligibility affecting daily communication will participate in this study. The patients will be randomly allocated to either speech therapy or a waiting list control group (1:1 ratio). Speech therapy using telerehabilitation will be provided for 8 weeks which consists of 12-16 sessions. The control group will receive deferred treatment after 8 weeks. The measurements will take place before the randomization (To), after 8 weeks (T1), and for the experimental group also after 24 weeks (T2). The primary outcome measure is quality of life, as measured using the total score on the PDQ-39. Secondary outcome measures include speech and voice, speech intelligibility, non-motor symptoms and caregiver burden. Hypothesis: The investigators hypothesize that patients in all disease stages can improve their speech intelligibility by using the explicit feedback from external cues provided by instructed caregivers plus a dedicated smartphone/ tablet app (the Voice Trainer app).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
Speech therapy, Telerehabilitation, Quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
The assessors will be blinded for treatment allocation.
Allocation
Randomized
Enrollment
214 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Speech therapy, right after T0 (baseline measurement).
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients will be on a waiting list for 8 weeks. After the primary endpoint (T1), patients will receive speech therapy.
Intervention Type
Other
Intervention Name(s)
Speech therapy
Intervention Description
Online speech therapy, delivered by specialized speech therapists. Speech therapy will be complemented by a real-time visual feedback app (the Voice Trainer app).
Primary Outcome Measure Information:
Title
Disease-specific health-related quality of life
Description
Parkinson's Disease Questionnaire (PDQ-39)
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1)
Secondary Outcome Measure Information:
Title
Speech quality
Description
Radboud Dysarthria Assessment (RDA)
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2)
Title
Voice quality
Description
Acoustic Voice Quality Index (AVQI)
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2)
Title
Voice handicap
Description
Voice Handicap Index (VHI)
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2)
Title
Severity of voice and speech complaints, reported by patient
Description
Radboud Oral Motor inventory for Parkinson's disease (ROMP)
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2)
Title
Severity of voice and speech complaints, reported by caregiver
Description
Radboud Oral Motor inventory for Parkinson's disease (ROMP), adapted to caregiver
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2)
Title
Speech intelligibility
Description
Dutch intelligibility test - sentence level (NSVO-Z)
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2)
Title
Caregiver burden
Description
Zarit caregiver Burden Interview Short Form (ZBI-12)
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2)
Title
Mood and anxiety
Description
Hospital Anxiety and Depression Scale (HADS)
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2). Minimum score = 0 (no anxiety or depression), maximum score = 42 (most anxiety or depression).
Title
Health-related quality of life
Description
EuroQol-5D (EQ-5D)
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2)
Title
Swallowing
Description
Maximum swallowing speed (timed test)
Time Frame
Baseline (T0), primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2)
Other Pre-specified Outcome Measures:
Title
Disease-specific health-related quality of life (follow-up)
Description
Parkinson's Disease Questionnaire (PDQ-39)
Time Frame
Primary endpoint after 8 weeks (T1), follow-up after 32 weeks (T2)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A diagnosis of idiopathic PD; Problems in intelligibility affecting daily communication (as indicated by the patient and/or the caregiver); A desire for improvement; willing and able to receive online treatment Exclusion Criteria: Recent (<1 year) speech therapy; Voice or speech problems due to other causes; Communication difficulties based on language problems without predominantly reduced intelligibility; inability to receive online treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bastiaan R Bloem, MD, PhD
Organizational Affiliation
Department of Neurology, Radboudumc, Nijmegen, the Netherlands
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radboud university medical center
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6500HB
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We will make relevant and anonymised data available in a validated database (DANS Easy).
IPD Sharing Time Frame
After publication of the main results of our trial.
IPD Sharing Access Criteria
Access to the data is restricted, meaning that researchers who are interested in re-use of the data are asked to contact the central contact person for permission. Approval is given after a signed agreement.
Citations:
PubMed Identifier
22895930
Citation
Herd CP, Tomlinson CL, Deane KH, Brady MC, Smith CH, Sackley CM, Clarke CE. Speech and language therapy versus placebo or no intervention for speech problems in Parkinson's disease. Cochrane Database Syst Rev. 2012 Aug 15;2012(8):CD002812. doi: 10.1002/14651858.CD002812.pub2.
Results Reference
background
PubMed Identifier
22895931
Citation
Herd CP, Tomlinson CL, Deane KH, Brady MC, Smith CH, Sackley CM, Clarke CE. Comparison of speech and language therapy techniques for speech problems in Parkinson's disease. Cochrane Database Syst Rev. 2012 Aug 15;2012(8):CD002814. doi: 10.1002/14651858.CD002814.pub2.
Results Reference
background
PubMed Identifier
35395953
Citation
Maas JJL, De Vries NM, Bloem BR, Kalf JG. Design of the PERSPECTIVE study: PERsonalized SPEeCh Therapy for actIVE conversation in Parkinson's disease (randomized controlled trial). Trials. 2022 Apr 8;23(1):274. doi: 10.1186/s13063-022-06160-9.
Results Reference
derived

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PERsonalized SPEeCh Therapy for actIVE Conversation

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