Comparison of Hip Range of Motion Values Among NCAA Division II Collegiate Athletes

June 17, 2016 updated by: Scott Cheatham, California State University, Dominguez Hills
The purpose of this study is to compare hip passive range of motion (ROM) among division II collegiate athletes in order to obtain normative data for future research. The investigators hypothesize that there will be a difference in passive hip ROM among the different genders and sports.

Study Overview

Status

Unknown

Detailed Description

Currently there is no normative data for hip passive ROM in apparently healthy NCAA division II collegiate athletes. This study will be the first study to develop preliminary normative data of hip passive ROM.

One hundred (N=100) student athletes (18-45 years) from California State University Dominguez Hills (CSUDH) will be recruited for this study via convenience sampling. Data collection will take place in the CSUDH sports medicine laboratory. Prior to testing, participants will fill out a screening questionnaire with questions that represent the exclusion criteria which will be used to determine ineligibility for this study.

Prior to participant recruitment and enrollment, a pilot study will be done on 10 participants to establish rater reliability using the methods mentioned below. After acceptable reliability is achieved, recruitment and enrollment will continue.

Participants who meet the inclusion criteria and consent to participate will be enrolled in the study. Participants will read and sign a CSUDH approved consent form prior to beginning data collection. Following consent, participants will also fill out a questionnaire to provide demographic information which includes age, height, weight, and leg dominance.

Following completion of the paperwork, all participants will undergo testing which will be conducted between the hours of 8am and 4pm. Each data collection session will last for approximately 20 minutes. Bilateral hip passive ROM data will be collected using the Noraxon computerized motion system. Participants will be lying in different positions on an examination table while the hip joints and lower extremities are moved into different positions and measured by the device which will touch the skin. Data will be collected and monitored by the examiner using the computerized system. The data collection protocol for both lower extremities are as follows:

  1. Supine measures (passive): hip external rotation, hip internal rotation
  2. Rest: 5-minute delay
  3. Seated measures (passive): hip external rotation, hip internal rotation
  4. Rest: 5-minute delay
  5. Prone measurements (passive): hip external rotation, hip internal rotation

Collected data will be transferred to SPSS v.22 (IBM SPSS, Chicago, IL). Means,standard deviations, 95% confidence intervals (95% CI), and ranges for participant descriptive data will be calculated. Passive Hip ROM values will be presented using degrees and percentages. Athlete gender and sport differences will be calculated using the ANOVA statistic. The p-value will be considered significant at the .05 level using a two-tailed test (α2 =.05).

Study Type

Observational

Enrollment (Anticipated)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 45 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Division II collegiate athletes (18-45) currently enrolled in school and participating on a sports team.

Description

Inclusion Criteria:

  • Healthy student collegiate athletes

Exclusion Criteria:

  • Presence of musculoskeletal, systemic or metabolic diseases that would affect lower extremity joint ROM or muscle function
  • Presence of any current or past muscle or joint pathology of the hip, knee, and/or ankle that would affect lower extremity joint ROM or muscle function
  • Inability to avoid exercise 4 hours prior to testing
  • Inability to avoid medications that may affect the outcome of lower extremity joint ROM or muscle function

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Division II Collegiate Athletes
Student athletes (18-45) currently enrolled and participating on a sports team.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Hip Joint Internal and External Rotation ROM
Time Frame: Baseline
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Scott W Cheatham, DPT, PhD, California State University, Dominguez Hills

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2016

Primary Completion (Anticipated)

January 1, 2017

Study Completion (Anticipated)

January 1, 2017

Study Registration Dates

First Submitted

June 16, 2016

First Submitted That Met QC Criteria

June 17, 2016

First Posted (Estimate)

June 20, 2016

Study Record Updates

Last Update Posted (Estimate)

June 20, 2016

Last Update Submitted That Met QC Criteria

June 17, 2016

Last Verified

June 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • 16-208

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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