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STIMPulseControl Ancillary Speech Study

STIMPulseControl Ancillary Speech Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06561919
Enrollment
60
Registered
2024-08-20
Start date
2024-09-05
Completion date
2028-07-15
Last updated
2025-12-02

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

Conditions

Impulse Control Disorder, Parkinson Disease

Keywords

Speech

Brief summary

Speech assessment is a substudy to the STIMPulseControl study (hereinafter referred to as the main study), where audio recordings of patients voices will be recorded as part of a speech analysis in the main study, for this optional ancillary study.

Detailed description

Speech of all study patients enrolled in the STIMPulseControl main study will be recorded at three points of time in a standardized way. Following this ancillary protocol, patients speech will be recorded at the baseline visit (preoperatively), at the 6-months visit and at the 12-months visit postoperatively. For the baseline speech assessment the same protocol will be performed in chronic medication conditions. At 12-month follow up, we will repeat the speech protocol in chronic medication and stimulation condition. The recordings will be done in each centre in a decentralized way and the audio files will be produced according to a standardized protocol, and assisted by a step-by-step guided speech recording software. Main aims and hypothesis for automated speech analysis study are safety measures for surgical interventions in PD assessment of parkinsonian (hypokinetic) motor speech features outcome after STN-DBS, assessment of dyskinetic (hyperkinetic) motor speech features outcome after STN-DBS, assessment of capsular speech features outcome after STN-DBS in PD emotional and cognitive speech outcomes to be used in surgical and pharmacological interventions in PD assessment of acoustic and linguistic speech features as proxy for behaviour and cognitive changes in PD, comparison of emotional and cognitive speech outcomes before and 1-year after STN-DBS + BMT vs BMT alone.

Interventions

PROCEDUREbilateral high frequency deep brain stimulation of the subthalamic neucleus combined with best medical treatment according to widely accepted expert consensus paper

Best medical treatment according to widely accepted expert consensus Paper

DRUGbest medical treatment for management of impulse control in Parkinson´s disease according to widely accepted expert consensus paper

Best medical treatment according to widely accepted consensus Paper

Sponsors

Czech Technical University in Prague
CollaboratorOTHER
Insel Gruppe AG, University Hospital Bern
CollaboratorOTHER
Philipps University Marburg
CollaboratorOTHER
University Hospital Schleswig-Holstein
CollaboratorOTHER
Amsterdam University Medical Centers (UMC), Location Academic Medical Center (AMC)
CollaboratorOTHER
Steffen Paschen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

Please refer to main study (STIMPulseControl KKS-313)

Exclusion criteria

Please refer to main study (STIMPulseControl KKS-313)

Design outcomes

Primary

MeasureTime frameDescription
Titel: PART 1: Assessment of parkinsonian motor speech features (hypokinetic dysarthria) outcome after STN-DBS12 monthsprimary aim: To globally assess motor speech features of PD change after STN-DBS intervention. Outcome: A compound score resulting from the normalized average of the main speech domains of hypokinetic dysarthria (i.e.phonation, articulation, prosody and timing) will be analyzed. For example, as proxy of phonation/voice quality, harmonics-to-noise ratio will be used. For the assessment of articulation changes, voice to onset (VOT) and Resonant frequency attenuation (RFA) will be assessed. Monopitch, will be assessed using the standard deviation of fundamental frequency (sdF0), while reduced intensity of speech variability or monoloudness will be assessed using the standard deviation of speech intensity (sdInt). To assess timing abnormalities seen in PD, prolonged pauses (PrLP), disrupting natural rhythm of speech, will be used.
Titel PART 2: Assessment of acoustic and linguistic speech features as proxy for behavior and cognitive changes in PD12 monthsprimary aim: To assess how paralinguistic speech content changes after STN-DBS intervention. Outcome: A compound score resulting from the normalized average of the main emotional paralinguistic features (such as pitch variability; duration of voiced segments, pause durations and intensity variability).

Secondary

MeasureTime frameDescription
PART I/B: Safety measures for surgical interventions in PD12 monthssecondary aim B: Comparison of paralinguistic speech outcomes before and 1-year after STN-DBS + BMT vs BMT alone. Outcome: Comparison of the rate of change of the compound score resulting from the normalized average of the main semantic features (such as content density, N-grams parameter, or moving-average type-token ratio).
PART II/C: Emotional and cognitive speech outcomes to be used in surgical and pharmacological interventions in PD12 monthssecondary aim C: Assessment of capsular speech features outcome after STN-DBS in PD. Outcome: A compound score resulting from the normalized average of the main speech features affected by capsular stimulation induced side-effects (such as net speech rate and pitch breaks during sustained phonation).
PART I/A: Safety measures for surgical interventions in PD12 monthssecondary aim A: Assessment of dyskinetic (hyperkinetic) motor speech features outcome after STN-DBS. Outcome: A compound score resulting from the normalized average of the main speech features affected by dyskinesia (such as intensity variability, breading capacity and spectral features variability).

Countries

Germany, Netherlands, Switzerland

Contacts

Primary ContactSteffen Paschen, MD
steffen.paschen@uksh.de0049 431 500 23819
Backup ContactGünter Deuschl, Prof. Dr.
g.deuschl@neurologie.uni-kiel.de0049 431 500 238956

Outcome results

None listed

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