Skip to content

Training Balance Among People With Neurodevelopmental Disabilities

Training Anticipatory Postural Adjustments Among People With Neurodevelopmental Disabilities

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04293120
Acronym
TAPAS
Enrollment
3
Registered
2020-03-03
Start date
2020-02-10
Completion date
2020-08-31
Last updated
2021-06-01

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

Conditions

Autism, Balance, Cerebral Palsy, Down Syndrome, Posture

Brief summary

This study is a case control pilot study to investigate the impact of a short-term intervention on training anticipatory postural adjustments in a population of people with neurodevelopmental disabilities.

Detailed description

Data will be collected by using a weighted pendulum to provide a posterior perturbation to test subjects' postural reactions pre and post-intervention. Intervention will include four sessions of weighted ball tosses/weighted tether ball stops to improve muscle activation patterns and efficiency. EMG sensors, 3D motion analysis, and force plates will be used to collect the necessary data.

Interventions

OTHERTraining with weighted ball

Participants will stop or catch a weighted ball

Sponsors

Universita di Verona
CollaboratorOTHER
University of Hartford
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Case control, matched on gender, age, and BMI

Eligibility

Sex/Gender
ALL
Age
8 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

Participants 1. Able to stand without assistance 2. Diagnosis of cerebral palsy, Down Syndrome, or Autism Spectrum Disorder 3. Able to stop weighted ball without falling 4. Able to follow directions Controls 1. Able to stand without assistance 2. No neurodeveloopmental disability 3. Able to stop weighted ball without falling 4. Able to follow directions

Exclusion criteria

1. Pregnancy 2. Unable to maintain standing when stopping a ball on a rope

Design outcomes

Primary

MeasureTime frameDescription
Muscle activation timingPre-intervention muscle activation timing will be assessed on the initial visit. Post-intervention muscle activation timing will be assessed immediately after the fourth training session, at most, 7 days later.Evaluation in change in muscle activation timing of anterior tibialis, soleus, gastroc, rectus femoris, biceps femoris, rectus abdominis using electromyography

Secondary

MeasureTime frameDescription
Muscle amplitude responsePre-intervention muscle amplitude response will be assessed on the initial visit. Post-intervention muscle amplitude response will be assessed immediately after the fourth training session, at most, 7 days later.Evaluation in change in amplitude of anterior tibialis, soleus, gastroc, rectus femoris, biceps femoris, rectus abdominis using electromyography

Countries

United States

Outcome results

None listed

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