Neural Mobilisation Effect on Calf Muscle

May 12, 2026 updated by: NITHIYAH MARUTHEY, INTI International University

The Effect of Neural Mobilization on Calf Muscle Length and Strength in Ballet Dancers: a Randomized Controlled Trial

The purpose of this study was to investigate Neural mobilisation effects on calf muscles length and strength is crucial to optimize ballet performance and prevent injuries.

Study Overview

Detailed Description

A randomized controlled trial is conducted with a total of 54 non-professional ballet dancers recruited from ballet studios across the Klang Valley following inclusion and exclusion criteria. Baseline measurement of calf muscle performance was conducted before randomization using knee-to-wall (KtW) test, handheld dynamometer (HHD) and Y-balance (YBT). Participants were allocated to experimental (NM and self-stretching) or control (self stretching) .

Study Type

Interventional

Enrollment (Actual)

54

Phase

  • Not Applicable

Contacts and Locations

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

Study Locations

    • Negeri Sembilan
      • Seremban, Negeri Sembilan, Malaysia, 71800
        • Inti International University

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

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Classical ballet trained female or male .
  • Subjects who are trained in classical ballet syllabus such as Royal Academy of Dance (RAD) Syllabus, The Classical Ballet Syllabus by Commonwealth Society of Teachers of Dancing (CSTD), Vaganova Syllabus and more.
  • Aged 13-23 years old
  • Dancers who took class/practice ballet for at least 3 times per week
  • Participated in ballet competition in recent 6 months

Exclusion Criteria:

  • Professional full time ballet dancers
  • Non-ballet dancers
  • Self-reported lower extremity injuries in the past 6 months prior to date of data collection
  • Subjects with existing musculoskeletal injuries might affect calf muscle performance
  • Involvement in other sports or physical training

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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Neural mobilisation group
neural mobilisation of tibial nerve and gastrocnemius stretching
the neural mobilisation was done with placement of participant's leg in hip flexion, knee extension, ankle dorsiflexion and eversion to load the nerve. Then leg is placed back to neutral position, with ankle naturally plantarflexed to unload the nerve. NM of tibial nerve was done in a total of 10 seconds each repetition, with 5 seconds each for loading and unloading of nerve. Then 12 repetition was done in one set, which amount to a total of 120seconds or 2 minute per set. A total of 3 sets was done on each leg, with a 1-minute resting interval after each set. NM was administered to participants in experimental group before their ballet class for 3 times a week lasting for 4 weeks.
Other Names:
  • nerve gliding
  • nerve tensioning
Participants was instructed to perform the classic wall stretch for gastrocnemius as self-stretching for a duration of 30 seconds each leg. It was done facing the wall and one leg had knee flexed in front while the other leg had knee extended behind. A 30 second hold was maintained at maximum stretched position by leaning forward while both soles of feet remain contact on the ground. Self-stretch was performed throughout the 4-week study duration before every ballet training or class.
Other Names:
  • calf self stretching
Active Comparator: Gastrocnemius stretching group
Participants was instructed to perform the classic wall stretch for gastrocnemius as self-stretching for a duration of 30 seconds each leg. It was done facing the wall and one leg had knee flexed in front while the other leg had knee extended behind. A 30 second hold was maintained at maximum tretched position by leaning forward while both soles of feet remain contact on the round. Self-stretch was performed throughout the 4-week study duration before every ballet training or class.
Participants was instructed to perform the classic wall stretch for gastrocnemius as self-stretching for a duration of 30 seconds each leg. It was done facing the wall and one leg had knee flexed in front while the other leg had knee extended behind. A 30 second hold was maintained at maximum stretched position by leaning forward while both soles of feet remain contact on the ground. Self-stretch was performed throughout the 4-week study duration before every ballet training or class.
Other Names:
  • calf self stretching

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
knee to wall test
Time Frame: From enrollment to the end of treatment at 4 weeks
The participants placed the testing foot onto the measuring tape with foot perpendicular to the wall while lunging or bending the knee to touch the wall. Then participants slide their foot further away from the wall as much as ossible while maintaining contact of knee to the wall as well as heel of foot on the floor. The calf muscle flexibility is evaluated with the measurement of distance from the great toe to the wall will be the maximum possible ankle dorsiflexion for the individual.
From enrollment to the end of treatment at 4 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Calf muscle strength
Time Frame: From enrollment to the end of treatment at 4 weeks
Calf muscle strength was measured using handheld dynamometer (HHD).The device was placed at the plantar aspect of metatarsophalangeal joint height and the body of HHD should be maintained perpendicular to the plane of ankle plantarflexion movement. Isometric contraction of ankle plantarflexor was done in maximum possible force for 5 seconds. Participant performed one trial to familiarize with the test, followed by 3 repetitions alternated on each leg with 1-minute resting interval.
From enrollment to the end of treatment at 4 weeks
Dynamic balance using Modified Star Excursion Balance Test (mSEBT)
Time Frame: From enrollment to the end of treatment at 4 weeks
Participants maintained their hands on the hip and reached tip of hallux to the maximal distance. The reaching foot were to avoid touching the ground and the heel of standing foot should remain on the ground. One trial on each direction was performed to familiarize with the test, followed by three trials with 1 minute resting interval. Normalize reach distance to lower limb length and normalized composite score were calculated to ultimately evaluate dynamic balance of an individual.
From enrollment to the end of treatment at 4 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: NITHIYAH MARUTHEY, Inti International University

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 (Actual)

August 20, 2024

Primary Completion (Actual)

January 15, 2026

Study Completion (Actual)

January 15, 2026

Study Registration Dates

First Submitted

May 6, 2026

First Submitted That Met QC Criteria

May 6, 2026

First Posted (Actual)

May 13, 2026

Study Record Updates

Last Update Posted (Actual)

May 14, 2026

Last Update Submitted That Met QC Criteria

May 12, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • INTI-IU/FHLS-RC/BPTHI/1NY12024

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

Upon careful consideration it will be decided to protect participants privacy

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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