NCT02595411

Brief Summary

The aim of the study is to investigate the reliability of the Melbourne Assessment.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jul 2015

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2015

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

November 2, 2015

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 3, 2015

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2016

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2016

Completed
Last Updated

February 7, 2017

Status Verified

February 1, 2017

Enrollment Period

1 year

First QC Date

November 2, 2015

Last Update Submit

February 6, 2017

Conditions

Cerebral PalsyStrokeTraumatic Brain InjuryMeningomyeloceleCentral Nervous System Diseases

Keywords

ChildrenRehabilitationUpper LimbAssessmentsOutcome Measures

Outcome Measures

Primary Outcomes (1)

  • Melbourne Assessment 2

    Assessment to measure unilateral upper limb function

    2 assessments within 1 week

Eligibility Criteria

Age30 Months - 20 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodProbability Sample
Study Population

Children with central motor disorders and impaired upper limb function

You may qualify if:

  • central motor disorders
  • ambulant or stationary patients of the Rehabilitation Center Affoltern am Albis
  • ability to understand test instructions
  • ability to sit upright for 25 minutes
  • minimal activity in the assessed upper limb

You may not qualify if:

  • severe visual and/or auditory problems
  • acute lesion in the to assessed upper limb
  • lack of compliance

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Children's Hospital Zurich, Rehabilitation Centre Affoltern am Albis

Affoltern am Albis, CH-8910, Switzerland

Location

MeSH Terms

Conditions

Cerebral PalsyStrokeBrain Injuries, TraumaticMeningomyeloceleCentral Nervous System Diseases

Condition Hierarchy (Ancestors)

Brain Damage, ChronicBrain DiseasesNervous System DiseasesCerebrovascular DisordersVascular DiseasesCardiovascular DiseasesBrain InjuriesCraniocerebral TraumaTrauma, Nervous SystemWounds and InjuriesNeural Tube DefectsNervous System MalformationsCongenital AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and Abnormalities

Study Officials

  • Hubertus van Hedel, PD Dr.

    University Children's Hospital Zurich, Rehabilitation Centre Affoltern am Albis

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 2, 2015

First Posted

November 3, 2015

Study Start

July 1, 2015

Primary Completion

July 1, 2016

Study Completion

December 1, 2016

Last Updated

February 7, 2017

Record last verified: 2017-02

Data Sharing

IPD Sharing
Will not share

Locations

CH(1)