NCT05652452

Brief Summary

The goal of this study is to explore the intervention effect of home-based neurodynamic slider program on hamstring flexibility. Fifty physically active male subjects will be randomly assigned to either performing a neurodynamic sliding technique (3x20 reps) or a static stretching protocol (3x30") on a daily basis for a 6-week period. Hamstring flexibility will be assessed by means of the Straight Leg Raise at baseline, immediately after the intervention and after 4 weeks follow up.

Trial Health

100
On Track

Trial Health Score

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

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2017

Status
completed

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

January 1, 2017

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2017

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2018

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

July 4, 2018

Completed
4.5 years until next milestone

First Posted

Study publicly available on registry

December 15, 2022

Completed
Last Updated

December 15, 2022

Status Verified

December 1, 2022

Enrollment Period

6 months

First QC Date

July 4, 2018

Last Update Submit

December 6, 2022

Conditions

Outcome Measures

Primary Outcomes (3)

  • Hamstring flexibility

    Straight leg raise by means of an app based goniometer

    at Baseline

  • Hamstring flexibility

    Straight leg raise by means of an app based goniometer

    6 weeks after intervention

  • Hamstring flexibility

    Straight leg raise by means of an app based goniometer

    4 weeks after retention period

Study Arms (2)

Neurodynamics

EXPERIMENTAL
Other: Neurodynamics

Static stretch

ACTIVE COMPARATOR
Other: Static stretch

Interventions

Subjects in the neurodynamic group performed the 'Seated Straight Leg Slider' (SSLS) (Fig.1). To execute this sliding technique, subjects assumed a seated slump position (thoracic and lumbar flexion) which they needed to maintain throughout the exercise. This SSLS consisted of alternating movements towards knee extension and ankle dorsiflexion (increase of neural tension) combined with cervical extension (decrease of neural tension) on one hand, and knee flexion and ankle plantar flexion (decrease neural tension) combined with cervical flexion (increase of neural tension) on the other. During this 6-week period, each subject in this neurodynamic slider group was instructed to perform 3 sets of 20 repetitions on a daily basis for 6 weeks.

Neurodynamics

Subjects in the control group were instructed to perform a standard standing static stretch with the heel of the dominant leg taking support on a chair. Then they had to move the pelvis into anteversion, simultaneously inducing a forward lean of the trunk, until the clear sensation of hamstring stretch was perceived at the posterior aspect of the thigh. Again, the execution of the exercise was thoroughly explained and evaluated by the researchers and subjects sent home with a comprehensive instruction guide and supporting pictures. Each subject was instructed to do 3 repetitions of 30 second static stretches on a daily basis during the 6-week intervention.

Static stretch

Eligibility Criteria

Sexmale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • male
  • aged between 18-30yrs
  • recreationally/competitively active
  • limited hamstring flexibility (Tight Hamstring Syndrome) (SLR≤75°)

You may not qualify if:

  • a history of any musculotendinous hamstring injury in the previous year
  • a history of neurological or orthopedic disorder affecting the lower extremities
  • a history of lumbar disc herniation; or (4) a history of a cervical whiplash injury

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 4, 2018

First Posted

December 15, 2022

Study Start

January 1, 2017

Primary Completion

July 1, 2017

Study Completion

July 1, 2018

Last Updated

December 15, 2022

Record last verified: 2022-12

Data Sharing

IPD Sharing
Will not share