Background <p>Subthalamic deep brain stimulation (STN-DBS) effectively treats motor symptoms in appropriately selected patients with Parkinson’s disease, but individual responses vary. Despite modern directional leads allowing more precise stimulation, optimal contact selection strategies have not yet been standardized. This study compares a standardized imaging-guided contact selection protocol to conventional clinical programming.</p> Methods <p>We designed a monocentric, randomized, double-blind crossover trial enrolling 30 people with Parkinson’s disease with bilateral directional STN-DBS. Participants will undergo both programming approaches: standardized imaging-guided contact selection targeting the dorsolateral STN and conventional contact selection through clinical test stimulations. Each configuration will be applied for 1 week. The primary outcome is patient preference after both treatments. Secondary outcomes include motor assessments (MDS-UPDRS III), accelerometric monitoring, and questionnaire-based quality of life measures (e.g., PDQ-39).</p> Discussion <p>This study addresses a critical gap in standardization of imaging-guided DBS programming. By using patient preference as the primary outcome, we aim to capture clinically meaningful differences that may not be detected with traditional motor scales. The crossover design balances statistical power with clinical feasibility in specialized care settings.</p> Trial registration <p>Deutsches Register für Klinische Studien DRKS00034229. Registered on May 27, 2024.</p>

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Comparative evaluation of standardized imaging-guided contact selection for subthalamic deep brain stimulation in Parkinson’s disease: study protocol for a randomized double-blind crossover trial

  • G. A. Brandt,
  • L. Piotrowsky,
  • J. N. Petry-Schmelzer,
  • C. van der Linden,
  • C. Schedlich-Teufer,
  • V. Visser-Vandewalle,
  • T. A. Dembek,
  • M. T. Barbe

摘要

Background

Subthalamic deep brain stimulation (STN-DBS) effectively treats motor symptoms in appropriately selected patients with Parkinson’s disease, but individual responses vary. Despite modern directional leads allowing more precise stimulation, optimal contact selection strategies have not yet been standardized. This study compares a standardized imaging-guided contact selection protocol to conventional clinical programming.

Methods

We designed a monocentric, randomized, double-blind crossover trial enrolling 30 people with Parkinson’s disease with bilateral directional STN-DBS. Participants will undergo both programming approaches: standardized imaging-guided contact selection targeting the dorsolateral STN and conventional contact selection through clinical test stimulations. Each configuration will be applied for 1 week. The primary outcome is patient preference after both treatments. Secondary outcomes include motor assessments (MDS-UPDRS III), accelerometric monitoring, and questionnaire-based quality of life measures (e.g., PDQ-39).

Discussion

This study addresses a critical gap in standardization of imaging-guided DBS programming. By using patient preference as the primary outcome, we aim to capture clinically meaningful differences that may not be detected with traditional motor scales. The crossover design balances statistical power with clinical feasibility in specialized care settings.

Trial registration

Deutsches Register für Klinische Studien DRKS00034229. Registered on May 27, 2024.