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Normative Biomechanical Measures of Reaching in Able-Bodied Adults

Normative Biomechanical Measures of Reaching in Able-Bodied Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05328947
Enrollment
40
Registered
2022-04-14
Start date
2022-07-14
Completion date
2023-06-29
Last updated
2024-07-16

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

Conditions

Individuals With Functional Limitations Which May Impact Their Forward Reach

Brief summary

A study to obtain normative values and repeatability measures during functional reaching tasks in able-bodied individuals with no functional limitations.

Detailed description

The study has three main aims: 1) Define the data collection methods, and calculate the repeatability, of joint angles, muscle activation magnitudes, seating pressure, foot pressure, and reach distance during seated and standing reaching activities. 2) Collect normative values of joint angles, muscle activation magnitudes, seating pressure, foot pressure, and reach distance during seated and standing functional reaching tasks in 40 participants with no functional limitations. Descriptive statistics will include calculating the mean, median, standard deviation, and range of the outcome variable values. 3) Compare joint angles, muscle activation magnitudes, seating pressure, foot pressure, and reach distance collected during a seated reaching task to those collected during a standing reaching task. The data collected may be used in the future as baseline reference and repeatability values of outcome measures against which to compare values from individuals with functional limitations to quantify their functional ability.

Interventions

OTHERModified Functional Reach and Functional Reach

Establishment of Modified Functional Reach Test (mFRT) and Function Reach Test (FRT) values for individuals with no functional impairments.

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 59 Years
Healthy volunteers
Yes

Inclusion criteria

• 20-59 years of age at time of enrollment

Exclusion criteria

* Failure to give consent or follow simple commands * Score of 7 or above on the QuickDASH Outcome Measure * Score of 5 or above on the Oswestry Low Back Disability Questionnaire * Score of 76 or below on the Lower Extremity Functional Scale * Diagnosis of a neuromuscular disorder (e.g., muscular dystrophy, multiple sclerosis, fibromyalgia) * Diagnosis of an inner ear balance disorder (e.g., benign paroxysmal positional vertigo) * Insufficient active range of motion of bilateral shoulders or hips that results in inability to perform forward or lateral reaching tasks * Any illness or condition which, based on the research team's assessment, will compromise the patient's ability to comply with the protocol, patient safety, or the validity of the data collected during this study

Design outcomes

Primary

MeasureTime frameDescription
Joint anglesOne data collection session, lasting approximately 4 hoursChange in measurements of joint angles at the shoulders, hips, knees, and ankles, measured in degrees.
ElectromyographyOne data collection session, lasting approximately 4 hoursMuscle activity over time and peak muscle activity, measured in volts. Muscles measured: erector spinae, rectus abdominis, gluteus maximus, gluteus medius, medial hamstring, vastus lateralis, gastrocnemius, and tibialis anterior.
Center of pressure excursionOne data collection session, lasting approximately 4 hoursPath of movement of the center of pressure applied by the buttocks to the seating surface and applied by the feet to the floor.
Seated and foot pressuresOne data collection session, lasting approximately 4 hoursPlot of pressure magnitude over the surface of the buttocks and the bottom of the feet.
Reach distanceOne data collection session, lasting approximately 4 hoursMeasurement of the furthest distance reached, measured in centimeters.

Countries

United States

Outcome results

None listed

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