Normative Biomechanical Measures of Reaching in Able-Bodied Adults

Sponsor
Mayo Clinic (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05328947
Collaborator
(none)
40
1
1
6
6.7

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: Modified Functional Reach and Functional Reach
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Normative Biomechanical Measures of Reaching in Able-Bodied Adults
Anticipated Study Start Date :
Jul 1, 2022
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Normal Controls

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

Outcome Measures

Primary Outcome Measures

  1. Joint angles [One data collection session, lasting approximately 4 hours]

    Change in measurements of joint angles at the shoulders, hips, knees, and ankles, measured in degrees.

  2. Electromyography [One data collection session, lasting approximately 4 hours]

    Muscle 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.

  3. Center of pressure excursion [One data collection session, lasting approximately 4 hours]

    Path of movement of the center of pressure applied by the buttocks to the seating surface and applied by the feet to the floor.

  4. Seated and foot pressures [One data collection session, lasting approximately 4 hours]

    Plot of pressure magnitude over the surface of the buttocks and the bottom of the feet.

  5. Reach distance [One data collection session, lasting approximately 4 hours]

    Measurement of the furthest distance reached, measured in centimeters.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 59 Years
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic Rochester Minnesota United States 55905

Sponsors and Collaborators

  • Mayo Clinic

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kristin Zhao, PhD, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT05328947
Other Study ID Numbers:
  • 22-000958
First Posted:
Apr 14, 2022
Last Update Posted:
Jun 30, 2022
Last Verified:
Jun 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jun 30, 2022