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Completed

NCT Number: NCT05193825

Evaluation of Remote DBS Programming.

Deep brain stimulation (DBS) represents the treatment of choice for advanced stages of Parkinson's disease (PD). Currently, adaptive closed-loop stimulation systems that apply disease-specific biomarkers, such as local field potentials (LFPs), are being actively examined to facilitate DBS programming. However, the most suitable feedback signal, still remains to be determined. The investigators previously tested the usefulness of the patient's subjective rating on a visual analogue scale (VAS) as a potential feedback signal for DBS adjustment and found that VAS-based programming lead to similar results as our standard approach. One of the practical advantages of using VAS-based programming strategies - in addition to saving time - is the principal applicability of such an approach to a remote programming setting, although a validation of such an approach is required. Within the scope of a prospective, randomized multicenter clinical trial (the REMOTE Trial), the investigators will examine the effectiveness and safety of VAS-based remote DBS programming in PD by using a novel and recently introduced software platform (Abbott NeurosphereTM Virtual Clinic) that allows for the programming through a smartphone-based video connection with the patient. Therefore, n = 50 PD patients undergoing STN-DBS surgery will be randomized and subsequent to surgery will have their IPG settings adjusted either during regular visits at the hospital or alternatively be programmed remotely through a VAS-based approach. Prior to surgery and after a 90 days follow-up period, we will assess specific clinical (MDS-Unified Parkinson's Disease Rating Scale = UPDRS, Parkinson's Disease Questionnaire-39 sum index = PDQ-39 SI, Beck Depression Inventory = BDI, Montreal Cognitive Assessment Scale = MOCA) parameters to determine the effectivity and safety of the two different strategies on the patient outcome and to correlate it with VAS ratings and MRI data. The results will support the examination of remote-based DBS programming and evaluate the patient's subjective judgment as a valid feedback signal.

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Key information

Age range

35 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ludwig Maximilian University Hospital

Munich, Bavaria, 81377, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 35 and 80 yrs.
  • Ability to communicate with the study physician and to understand the requirements of the study
  • Idiopathic Parkinson's Syndrome; IPS (according to MDS-Criteria)
  • Implantation of a DBS device for the stimulation of the subthalamic nucleus (STN) to treat PD.

Exclusion criteria

  • Any inability to communicate with the study physician and to understand the requirements of the study
  • Exclusion criteria of an idiopathic Parkinson's syndrome (IPS)
  • Fulfills the criteria of dementia (according to the International Classification of Diseases (ICD) 10)

Treatment and study plan

Remote Programming

Device

Patients in the experimental group (Group B) will have their internal pulse generators (IPGs) adjusted through a novel software that allows for remote DBS programming (NeurosphereTM Virtual Clinic)

Standard Programming

Device

Patients in the active comparator group (Group A) will have their internal pulse generators (IPGs) adjusted through a standard procedure at their caregivers institution.

Primary outcomes

  1. Change in UPDRS-III (Stimulation ON/Medication ON = STIM-ON/MED-ON)

    Time frame: Assessed at Day 90

    Part III of the MDS-Unified Parkinson's Disease Rating Scale (Range 0-128 pts. with high values indicating a more severe disease symptoms)

Secondary outcomes

  1. Change in UPDRS-I

    Time frame: Assessed at day -1 and +90 (day 0 = implantation of DBS electrodes)

    Part I of the MDS-Parkinson's Disease Rating Scale (Range 0-52 pts. with high values indicating more severe disease symptoms)

  2. Change in UPDRS-II

    Time frame: Assessed at day -1 and +90 (day 0 = implantation of DBS electrodes)

    Part II of the MDS-Parkinson's Disease Rating Scale (Range 0-52 pts. with high values indicating more severe disease symptoms)

  3. Change in UPDRS-IV

    Time frame: Assessed at day -1 and +90 (day 0 = implantation of DBS electrodes)

    Part IV of the MDS-Parkinson's Disease Rating Scale (Range 0-24 pts. with high values indicating more severe disease symptoms)

  4. Change in PDQ-39-SI

    Time frame: Assessed at day -1 and +90 (day 0 = implantation of DBS electrodes)

    Parkinson's Disease Questionnaire-39 Sum Index (Range 0-100 pts. with high values indicating more severe disease symptoms)

  5. Change in Patient Rating (Patient Diary)

    Time frame: Assessed on a weekly basis by the patient between day +5 and +90 (day 0 = implantation of DBS electrodes)

    Number of hours spent with bothersome dyskinesia or in a reduced mobility state (OFF)

  6. Number of visits at the the hospital or remotely

    Time frame: Assessed at day +90 (day 0 = implantation of DBS electrodes)

    Number of doctor-patient contacts either in person at the hospital (Group A) or remotely (Group B)

  7. Change in TEED

    Time frame: Assessed at day +5 and +90 (day 0 = implantation of DBS electrodes)

    Total Electrical Energy Delivered by the IPG; TEED (1s) = (voltage2 × frequency × pulsewidth) / impedance (1s)

Sponsors and collaborators

Lead sponsor

Thomas Köglsperger

Other

Collaborators

  • Friedrich-Alexander-Universität Erlangen-Nürnberg
  • Heinrich-Heine University, Duesseldorf
  • University Hospital Muenster
  • Universitätsklinikum Hamburg-Eppendorf
  • Universitätsklinikum Leipzig

Registry information

Official study title

Evaluation of a Visual-Analog Scale (VAS) for Remote DBS Programming

Acronym: REMOTE

Important dates

Study start
2022
Primary completion
2024
Study completion
2025
First posted
Jan 18, 2022
Registry last updated
Aug 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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