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Testing personalised brain stimulation during rehabilitation

Researchers investigate an early-stage approach that adjusts brain stimulation to support rehabilitation.

Testing a treatment or activity · Study reference: NCT07082595

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)
2025-07-07
Main measurements finished (planned)
2028-03-31
Study finished (planned)
2028-03-31

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?

Age 18 years and over · 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: * Idiopathic Parkinson's disease with gait and postural stability deficits * ≥18 years of age * UPDRS III gait scores 1-3 * UPDRS III postural instability scores 1-3 * Prescribed rehabilitation therapy * Informed consent as documented by signature * Adjustments in dopaminergic medication and DBS stimulation to improve Exclusion Criteria: * Cognitive impairment, Montreal Cognitive Assessment (MoCa) \< 20 * Other neurological or medical condition that caused sustained clinically relevant gait and/or postural stability deficits * History of a physical or neurological condition that interferes with study procedures * Social and/or personal circumstances that interfere with the ability to return for assessments * Patients taking benzodiazepines or Z-drugs that have a significant effect on sleep EEG * Recent DBS implant (≤ 6 months) * Inability to perform outcome assessments without walking aid * Skin disorders/problems/allergies in face/ear area that could worsen with electrode application (e.g. nickel allergy)
Full study name & original research details

Official study title

Personalized Stimulation Loop for Neurorehabilitation in Parkinson: a Proof-of-principle Study

Original description

Parkinson's disease (PD) is a neurodegenerative disease that affects about 1% of the elderly population and accounts for substantial disability and health care costs. Disability is largely driven by mobility deficits caused by impaired gait. Effective treatments are available to restore lower limb function and improve gait, but response to treatment varies greatly from patient to patient and often shows only small effect sizes. Addressing this heterogeneity requires personalization, a concept referred to precision neurorehabilitation. StimuLOOP.PD-Sleep intends to foster structured and reproducible methods for precision neurorehabilitation of gait in PD. The investigators will conduct a proof-of-concept study to investigate a sleep intervention tailored to the individual patient in the context of motor rehabilitation. • Targeted auditory stimulation during sleep (TASS): The investigators aim to reactive rehabilitation-related memories through presentation of auditory stimuli during sleep with the goal of promoting motor memory consolidation into stable motor commands. The investigators will leverage TASS to enhance consolidation of the movement patterns that are learned during rehabilitation. The investigators expect that this intervention will lead to greater gains in functional walking ability and balance. Beyond demonstrating a proof-of-concept for novel methods of applying TASS stimulation in the context of neurorehabilitation, positive results of this project may have implications for neurorehabilitation treatment in general by providing first insights into the benefits and interplay of TASS with a rehabilitation.

Conditions reported: Parkinson Disease

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
TASS Intervention (Sham); TASS Intervention (Verum)
Phases
NA
Sponsor
University of Zurich
Start date reported by registry
2025-07-07 (actual)

Registry updated: 2025-07-24 · Status last verified by the registry submitter: 2025-07

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.

Christian Baumann, Prof. Dr. med. · +41 44 255 00 02 · christian.baumann@usz.ch

Angelina Maric, Dr. phil. · + 41 255 86 15 · angelina.maric@usz.ch

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 of Zurich

Zurich, Canton of Zurich, Switzerland

Recruiting

Angelina Maric, Dr. phil. · +41 255 86 15 · angelina.maric@usz.ch

Yannik Rottenberger, MSc · +41 255 56 45 · yannik.rottenberger@usz.ch

Angelina Maric, Dr. phil.

William R. Taylor, Prof. Dr.

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.