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CompletedNCT04770987Updated Jul 22, 2021

Lateral Neck Flexor Endurance and Hyperlaxity

An observational study in Physical Endurance, Hypermobility, Joint and Muscular Weakness, sponsored by University of Hartford. Completed at 1 site in United States. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-07-22.

Sponsored by University of Hartford · Observational

Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
60
Ages
18 Years to 60 Years
Sex
All
01

Study summary

The lateral neck flexor endurance test has been proposed to assess for unilateral muscular deficits. It is not known if individuals with hyperlaxity have different muscular endurance than individuals without hyperlaxity.

Read the detailed description

Thirty individuals with systemic hyperlaxity as determined with the Beighton scale will be assessed for lateral neck flexor endurance and compared to age and gender matched controls. Basic demographic information will be collected, and all individuals will report Neck Disability Index (NDI) and Numeric Pain Rating Scales (NPRS) for their neck, as well duration of any neck pain. All participants will then undergo testing of lateral neck flexor muscle endurance, repeated twice on each side. Average hold times will be compared for individuals with hyperlaxity (5 or greater on Beighton scale) and the healthy age and gender matched controls. Analysis will also include covariates of NDI scores, pain scores, and chronicity of symptoms.

02

Conditions studied

  • Physical Endurance
  • Hypermobility, Joint
  • Muscular Weakness

Keywords

  • neck musculature
  • endurance
  • tests and measures
03

In context

Muscle Weakness

601 studies on the registry are indexed under Muscle Weakness; 99 are open to participants now.

This study's enrollment of 60 is below the median of 98 across 144 observational studies indexed under Muscle Weakness.

Browse Muscle Weakness studies →

Lead sponsor

University of Hartford is the lead sponsor of 16 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Individuals between the ages of 18-60 with and without systemic hyperlaxity

Inclusion criteria

systemic hyperlaxity of 5 or greater on Beighton Index, healthy age/gender matched controls

Exclusion criteria

Exclusion Criteria:

  • neck pain that spreads into the arms;
  • whiplash injury within the last 6 weeks;
  • diagnosed neuropathy or other nervous system disorders;
  • a history of spinal surgery in their neck;
  • fibromyalgia;
  • insulin dependent diabetes;
  • involved in legal activity regarding neck pain
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
60 participants (actual)
Patient registry
No

Groups and cohorts

  • hyperlaxity

    30 individuals with systemic hyperlaxity as defined by a score of 5 or greater on the Beighton Hypermobility Scale

    Other: lateral neck flexor endurance test

  • control

    30 healthy, age and gender matched individuals without hyperlaxity

    Other: lateral neck flexor endurance test

Interventions

  • Otherlateral neck flexor endurance test

    Individuals will maintain the head in a neutral position off the ground in sidelying for as long as possible.

06

What researchers measure

Primary outcomes

  1. lateral neck flexor endurance

    maximum hold time

    Time frame: single testing session at enrollment

Secondary outcomes

  1. Beighton Hyperlaxity Scale

    Assessment of systemic hyperlaxity, 0-9 points, higher indicates greater hyperlaxity

    Time frame: at enrollment

  2. Neck Disability Index

    Questionnaire assessing impact of neck symptoms on function, 0-100 points, higher score indicates greater disability

    Time frame: at enrollment

  3. Numeric pain rating scale

    assessment of neck pain, 0-10 with higher indicating greater levels of pain

    Time frame: at enrollment

07

Study locations

1 site
  • University of Hartford
    West Hartford, Connecticut 06117, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 22, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04770987
Lead sponsor
University of Hartford
Responsible party
Sponsor
First posted
Feb 25, 2021
Start date
Feb 26, 2021
Primary completion
Jul 16, 2021
Completion
Jul 16, 2021
Last update
Jul 22, 2021

Study contacts

Brian Swanson, PT, DSc
principal investigator · University of Hartford

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2021. You cannot join it, but the record below documents what was studied.

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