NCT06249880

Brief Summary

The objective of this project is to collect baseline data from a normative population of 20 children that gender and age matches the population of patients expected to be treated by Mary Bridge Children's Research \& Movement Lab.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
30mo left

Started Mar 2024

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress48%
Mar 2024Dec 2028

First Submitted

Initial submission to the registry

January 24, 2024

Completed
15 days until next milestone

First Posted

Study publicly available on registry

February 8, 2024

Completed
22 days until next milestone

Study Start

First participant enrolled

March 1, 2024

Completed
3.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2027

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2028

Last Updated

March 9, 2026

Status Verified

March 1, 2026

Enrollment Period

3.8 years

First QC Date

January 24, 2024

Last Update Submit

March 5, 2026

Conditions

Keywords

Motion AnalysisKineticsKinematics

Outcome Measures

Primary Outcomes (1)

  • Observation-based movement analyses

    The purpose of this normative data collection study is to collect baseline data from a normative population of children/adolescents using force plates and 3D markerless motion capture. Together these are used to calculate a normative range of body position and joint angles (kinematics), as well as joint loads and ground reaction forces (kinetics) during prescribed activities.

    Baseline

Study Arms (1)

Normative

40 neurotypical pediatric subjects

Other: Observation

Interventions

This project seeks to recruit 20 male and 20 female typically developing individuals, between the ages of 3 and 25 years of age. Non-invasive measurements of movement patterns (motion analysis and force plate data) will be collected during bipedal gait.

Normative

Eligibility Criteria

Age3 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Subjects will be recruited from the regional community, including convenience sample of children. Subjects will be recruited by word of mouth, posted flyers, and advertised through the RML website and MB social media.

You may qualify if:

  • Ambulate independently and without the use of assistive devices or orthoses.
  • Willing and interested in participating.

You may not qualify if:

  • Neuromuscular disorders such as cerebral palsy, muscular dystrophy, myotonic dystrophy, spinal muscular atrophy, peripheral neuropathy, or other generalized muscle and/or nerve issues.
  • Evidence of developmental delays, muscle weakness, decreased muscle tone, joint stiffness, muscle or bone deformity.
  • Currently using or has a history of using assistive technology devices, bracing/orthoses, manual or powered mobility equipment.
  • History of premature birth.
  • Currently or has a history of taking medication or pharmaceutical treatment related to musculoskeletal side-effects/scenario/diagnosis.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mary Bridge Children's Therapy Unit - Research & Movement Lab

Puyallup, Washington, 98372, United States

RECRUITING

MeSH Terms

Conditions

Precursor Cell Lymphoblastic Leukemia-Lymphoma

Interventions

Observation

Condition Hierarchy (Ancestors)

Leukemia, LymphoidLeukemiaNeoplasms by Histologic TypeNeoplasmsHematologic DiseasesHemic and Lymphatic DiseasesLymphoproliferative DisordersLymphatic DiseasesImmunoproliferative DisordersImmune System Diseases

Intervention Hierarchy (Ancestors)

MethodsInvestigative Techniques

Study Officials

  • Brenna Brandsma

    Mary Bridge Chidlren's

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Brenna Brandsma, PT, DPT, PCS

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physical Therapist

Study Record Dates

First Submitted

January 24, 2024

First Posted

February 8, 2024

Study Start

March 1, 2024

Primary Completion (Estimated)

December 1, 2027

Study Completion (Estimated)

December 1, 2028

Last Updated

March 9, 2026

Record last verified: 2026-03

Locations