NCT07721220

Brief Summary

This study explores the acute effects of neurodynamics, an intervention commonly used by physical therapist to improve nerve mobility and decrease pain, on the strength and muscular endurance in the athletic population. This study aims to find if these interventions can maintain or promote strength and endurance in the hamstrings. The studies results will help physical therapist better prescribe exercise and hands-on treatment for hamstring and sciatic nerve related conditions and injuries.

Trial Health

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Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
45

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2026

Shorter than P25 for not_applicable

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 15, 2026

Completed
16 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2026

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

July 16, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

July 22, 2026

Completed
Last Updated

July 22, 2026

Status Verified

July 1, 2026

Enrollment Period

16 days

First QC Date

July 16, 2026

Last Update Submit

July 20, 2026

Conditions

Keywords

hamstringsciatic nerveathlete

Outcome Measures

Primary Outcomes (1)

  • Isometric Strength

    Isometric strength of the hamstrings in knee flexion.

    From initial strength and endurance test, to the post intervention strength and endurance test, assessed during a single study visit, assessed up to 30 minutes.

Secondary Outcomes (1)

  • Endurance Ratio (isokinetic)

    From initial endurance test to post intervention endurance test, during a single study visit, assessed up to 30 minutes.

Study Arms (3)

Sliders

ACTIVE COMPARATOR

Manually applying slider technique of neurodynamics.

Other: Sciatic Slider

Tensioners

ACTIVE COMPARATOR

Manually applied tensioner, neurodynamic technique

Other: Sciatic Tensioner

Mechanically Loaded Neurodynamics

EXPERIMENTAL

Externally loaded neurodynamic intervention in the slider technique.

Other: Mechanically loaded neurodynamic sciatic flossDevice: Elastic Resistance Band

Interventions

Elastic resistance band was used to provide submaximal resistance during the mechanically loaded neurodynamic intervention.

Mechanically Loaded Neurodynamics

Loading the nerve, by placing tension on both ends of the nerve, isometrically at end range of motion.

Tensioners

Mobility of a nerve, by placing tension on one end of the nerve and slacking (removing) tension off the other side of the nerve, through a full range of motion.

Sliders

Placing tension on one end of the nerve while taking the tension off the other end, under external load of an elastic resistance band.

Mechanically Loaded Neurodynamics

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Participants must be between 18 and 30 years of age.
  • Must be able to read, understand, and provide informed consent, in English.
  • Must be currently participating in an organized sport (e.g. collegiate, club, or competitive recreational level) or engaging in structured resistance training and athletic conditioning for recreational sports events (e.g 5k, marathon, Crossfit, Hyrox, etc).
  • Medically stable with no known contraindications to physical exertion.
  • Cleared for participation in strength or maximal-effort isometric testing.
  • Be able to perform lower extremity isometric testing without pain that limits maximal effort.
  • Must have 2 lower extremities capable to producing full range knee flexion and extension range of motion.
  • No medical condition that significantly alters lower extremity neuromuscular performance.
  • No history of lower extremity surgery in the past 12 months.

You may not qualify if:

  • Individuals younger than 18 or older than 30.
  • Acute lower extremity injury in the last 12 weeks.
  • Lower extremity surgery within the last 12 months.
  • Pain in either lower extremity that would limit maximal physical exertion.
  • History of neurological disorders, including but not limited to: Neuropathy, Stoke, MS, Parkinson's Disease, etc.
  • Use of medications that significantly impact neuromuscular performance, strength or fatigue.
  • No supplementation that affects neuromuscular performance, strength, or fatigue.
  • Unable to read and understand English.
  • Not in a vulnerable population: Pregnant, mentally or physically challenged, cognitively impaired.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

High Point University

High Point, North Carolina, 27268, United States

RECRUITING

MeSH Terms

Conditions

Intervertebral Disc Displacement

Condition Hierarchy (Ancestors)

Spinal DiseasesBone DiseasesMusculoskeletal DiseasesHerniaPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Study Officials

  • Tommy Wyatt, DPT

    High PointUniversity

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Dr. Tommy Wyat, DPT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr. Tommy Wyatt

Study Record Dates

First Submitted

July 16, 2026

First Posted

July 22, 2026

Study Start

June 15, 2026

Primary Completion

July 1, 2026

Study Completion

July 1, 2026

Last Updated

July 22, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will share

The raw pre and post isometric and isokinetic endurance ratio data for each participant will be shared. Along with the intervention leg, testing order, intervention provided, level of athletic participation, primary sport activity, age, sex.

Shared Documents
STUDY PROTOCOL, SAP
Time Frame
From study end date, for 3 years following.
Access Criteria
Yes, individual participant data that underlie the results reported in this article, after de-identification (text, tables, figures, and appendices), will be shared. Information will be available to researchers who provide a methodologically sound proposal to achieve aims in the approved proposal. Data will be available beginning 3 months and ending 36 months following article publication. Supporting documents including the study protocol and statistical analysis plan will also be available. Requests should be directed to twyatt2@highpoint.edu

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