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Crossmodal Learning in Therapeutic Processes (Task 2-2)

SFB TRR 169/A3 (2.FP) Crossmodal Learning in Health and Neurological Disease: Neurocomputational Representation and Therapeutic Application (Task 2-2)

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05262712
Enrollment
23
Registered
2022-03-02
Start date
2021-04-14
Completion date
2023-03-13
Last updated
2023-05-17

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

Conditions

Sensory Ataxia

Keywords

Vibro-tactile Stimulation, Neurorehabilitation, Ataxia

Brief summary

Interventional study of the effects of vibro-tactile feedback on behavioral deficits and learning during motor training in patients with sensory ataxia.

Interventions

Vibro-tactile stimulation will be administered to the feet of participants via C2 tactors (diameter: 3.05 cm, height: 0.79 cm, operating frequency: 200-300 Hz see https://www.eaiinfo.com/tactor-info/). Vibro-tactile stimulation will be triggered by force-sensing resistors (TEA CAPTIV T-SENS FSR, see https://www.teaergo.com/products/tea-captiv-t-sens-fsr/).

OTHERPlacebo Control

Devices mounted, no stimulation

Sponsors

German Research Foundation
CollaboratorOTHER
National Natural Science Foundation of China
CollaboratorOTHER_GOV
Universitätsklinikum Hamburg-Eppendorf
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Assessment, motor training, data analyzes and group allocation are done by different persons. Participants as well as the assessor, the trainer and the investigator are blinded to the group allocation.

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Electrophysiological diagnosis of sensory ataxia * Age \>= 18, \<=80 * Existing declaration of consent

Exclusion criteria

* Pregnancy * Lacking capacity for consent

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Timed Up-and Go TestOne day before (baseline) and one day after seven days of motor trainingThe Timed Up and Go test is a clinical test to assess a patient's mobility and risk of falling.

Secondary

MeasureTime frameDescription
Change from baseline in 10-Meter-Walk TestOne day before (baseline) and one day after seven days of motor trainingThe 10-Meter-Walk Test is a performance measure used to assess walking speed in meters per second over a short distance. It can be employed to determine functional mobility and gait.
Change from baseline in Berg-Balance-ScaleOne day before (baseline) and one day after seven days of motor trainingThe Berg-Balance-Scale (BBS) is used to determine a patient's ability to safely balance during a series of predetermined tasks. It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function.
Change from baseline in Postural-Sway TestOne day before (baseline) and one day after seven days of motor trainingThe Postural-Sway Test is a common test of quiet stance balance.

Countries

Germany

Outcome results

None listed

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