Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
ID06617884

Comparison of Two Home-based Gait and Balance Trainings With Different Frequencies in Patients With Parkinson's Disease and Ataxia

Led by Forschungszentrum Juelich · Updated on 2025-08-13

80

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

F

Forschungszentrum Juelich

Lead Sponsor

H

Heinrich-Heine University, Duesseldorf

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying patients with movement disorders, specifically cerebellar ataxia or idiopathic Parkinson's disease, to evaluate two different home-based video training programs designed to improve gait and balance. This experimental study uses a parallel design and includes patients who can walk independently for at least two minutes. The goal is to see if varied frequencies and durations of training affect gait and balance improvements, compared to a control group without training. Participants are randomly assigned to one of three groups: one group trains at home four times a week for 20 minutes per session, another group trains twice a week for 40 minutes per session, and a control group receives no additional training during the study. All training is video-based and includes exercises for strength, coordination, and flexibility. The study includes a one-week familiarization phase without training, followed by a three-week training phase and subsequent follow-up visits. Throughout the study, participants visit the study site three times and undergo gait and balance assessments using force plates and motion capture systems. They may also record movement data on their smartphones at home to capture everyday movement patterns. Researchers measure outcomes such as gait velocity and various balance and mobility scores. Safety is monitored, especially for fall risk, and participants can withdraw at any time. The entire study spans several weeks, including the training and follow-up periods.

CONDITIONS

Brief Title

Home-based Gait and Balance Training in Patients With Movement Disorders

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of cerebellar ataxia or idiopathic Parkinson's syndrome
  • Ability to walk a distance of four meters unhindered at home
  • Age between 18 and 75 years
Not Eligible

You will not qualify if you...

  • Other diseases affecting motor skills
  • Severe primary psychiatric illnesses
  • Current drug or alcohol addiction
  • Consumptive diseases
  • Poor general health condition
  • Increased risk of falling (falling at least once per week or as assessed by a physician)
  • Patients unable to give consent or under official custody
  • Parkinson's patients unable to be measured during the medication on-phase approximately two hours after medication intake
  • Incapacitated patients in official or court custody or unable to give consent
  • Increased risk of falling
  • Poor general condition
  • Current drug or alcohol dependency
  • Consumptive illnesses
  • Severe psychiatric illnesses
  • Other motor skill affecting diseases
  • For Parkinson's patients, inability to perform measurements during the on-phase of medication approximately two hours after intake
  • Patients unable to give consent or under legal custody (duplicated criteria merged for clarity, listed once in exclusion criteria as per source)

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 3 weeks

Participants perform home-based, video-guided gait and balance training with different frequencies to improve their movement. The training includes strength, coordination, and flexibility exercises tailored to each participant.

Training performed at home 4 times per week for 20 minutes or 2 times per week for 40 minutes, depending on group assignment

Follow-up

Duration - Up to 4 weeks after treatment

Participants continue with no additional training during this period. Patients in the control group do not perform training but have access to the training material after the study ends.

2 study visits (in-person) after training phase

Trial Site Locations

Total: 1 location

1

Universitätsklinikum Düsseldorf, Institut für Klinische Neurowissenschaften und Medizinische Psychologie

Düsseldorf, North Rhine-Westphalia, Germany, 40225

Actively Recruiting

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Research Team

M

Martina Minnerop, PD Dr. med.

C

Clara Rentz, M. Sc.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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