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Recording speech alongside a brain stimulation study

Researchers analyse voice recordings from people taking part in a Parkinson’s study of brain stimulation and impulse-control problems.

Testing a treatment or activity · Study reference: NCT06561919

Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓

This registry record was last updated over six months ago, or its update date is missing. Recruitment may have changed. Confirm with the team before making plans.

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Looking for volunteers

Start (reported actual date)
2024-09-05
Main measurements finished (planned)
2027-07-15
Study finished (planned)
2028-07-15

Planned dates can move. A study finishing does not tell us when a paper will be published.

No results summary has been confirmed in the registry records we imported. See connected papers below; we keep checking after recruitment ends.

Changes we have recorded
  • 2026-10-11 — recruiting

These are dates we observed a change, not necessarily the dates it happened.

Papers connected to this study

No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.

Who can join?

Ages 18 years to 70 years · Does not accept healthy volunteers

These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.

Read all the rules for taking part

Sex eligibility reported by registry: all

Inclusion Criteria: Please refer to main study (STIMPulseControl KKS-313) Exclusion Criteria: Please refer to main study (STIMPulseControl KKS-313)
Full study name & original research details

Official study title

STIMPulseControl Ancillary Speech Study

Original description

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.

Further description from the registry

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.

Conditions reported: Parkinson Disease; Impulse Control Disorder

Registry records for this study

Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.

Study type
Interventional
Interventions
bilateral high frequency deep brain stimulation of the subthalamic neucleus combined with best medical treatment according to widely accepted expert consensus paper; best medical treatment for management of impulse control in Parkinson´s disease according to widely accepted expert consensus paper
Phases
NA
Sponsor
Steffen Paschen
Start date reported by registry
2024-09-05 (actual)

Registry updated: 2025-12-02 · Status last verified by the registry submitter: 2025-12

Registry records retrieved 2026-10-13 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.

Contact the research team

Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.

Steffen Paschen, MD · 0049 431 500 23819 · steffen.paschen@uksh.de

Günter Deuschl, Prof. Dr. · 0049 431 500 238956 · g.deuschl@neurologie.uni-kiel.de

Study locations

Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.

University Hospital Cologne

Cologne, Germany

Recruiting

Michael Barbe, MD

University Hospital Carl Gustav Carus

Dresden, Germany

Recruiting

Bjoern Falkenburger, Prof.

University Hospital Duesseldorf

Düsseldorf, Germany

Recruiting

Alfons Schnitzler, Prof.

University Medical Center Hamburg-Eppendorf

Hamburg, Germany

Recruiting

Monika Poetter-Nerger, MD

University Hospital Schleswig-Holstein (UKSH), Campus Kiel

Kiel, Germany

Recruiting

Steffen Paschen, MD

University Hospital of Giessen and Marburg (UKGM), Campus Marburg

Marburg, Germany

Recruiting

David Pedrosa, MD

Charité Campus Mitte

Mitte, Germany

Recruiting

Patricia Krause, MD

University Hospital Tuebingen

Tübingen, Germany

Recruiting

Daniel Weiss, Prof.

University Hospital Wuerzburg

Würzburg, Germany

Recruiting

Jens Volkmann, Prof.

Amsterdam University Medical Center

Amsterdam, Netherlands

Recruiting

Rob MA De Bie, Prof.

Annabel von der Weide, MD

University Hospital of Bern (Inselspital)

Bern, Switzerland

Recruiting

Ines Debove, MD

Paul Krack, Prof.

University Hospital Zuerich (USZ)

Zurich, Switzerland

Recruiting

Lennart Stieglitz, Prof.

Fabian Buechele, MD

Facility not reported

Germany

Status not reported

Facility not reported

Netherlands

Status not reported

Facility not reported

Switzerland

Status not reported

The original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.