NCT05707117

Brief Summary

The aim of this research is to determine effects tendon neuroplastic training on strength, pain, and function in lateral epicondylitis. Randomized controlled trials will be conduct in National Institute of Rehabilitation Medicine Islamabad and Lady Reading Hospital Peshawar. The sample size is 34. The subjects will be divided in two groups, 17 subjects in tendon neuroplastic training group and 17 subjects will be assigned to conventional exercises group. Study duration is of one year. Sampling technique applied will be non-probability convenient sampling technique. Only 20-45 years old patients diagnosed with lateral epicondylitis will be included. Tools used in the study are Numeric pain scale, Dynamometer for grip strength and Patient rated tennis elbow evaluation for functional status.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
34

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

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, 2023

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

January 22, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

January 31, 2023

Completed
20 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 20, 2023

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 25, 2023

Completed
Last Updated

May 6, 2023

Status Verified

May 1, 2023

Enrollment Period

2 months

First QC Date

January 22, 2023

Last Update Submit

May 3, 2023

Conditions

Keywords

Lateral EpicondylitisTendon neuroplastic trainingstrength training

Outcome Measures

Primary Outcomes (1)

  • Numeric pain Rating scale (NPRS)

    The NPRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain. The common format is a horizontal bar or line

    4th week

Secondary Outcomes (2)

  • Patient rated tennis elbow evaluation (functional status).

    4th week

  • Dynamometer

    4th week

Study Arms (2)

Group A: Tendon neuroplastic training (TNT)

EXPERIMENTAL

the strength training of the wrist extensors are being done with the help of an externally pace device

Other: Tendon neuroplastic training (TNT)

Group B: Conventional treatment

ACTIVE COMPARATOR

static stretching and myofascial release on wrist extensors

Other: group B Conventional treatment

Interventions

Subjects will attend physical therapy for three non-consecutive days per week for a total 4 consecutive weeks. Exercise would involve isolated flexion, extension with a dumbbell. This exercise would be paced with external audio/visual cue on smart phone using proMetronome app. Patients will listen to the sound and track the movement of metronome with the eyes. Pace of metronome will be set at 20 beats per minute such that each beat will be 3 sec apart. This will allow a 3sec concentric and 3 sec eccentric phases.4 sets of 8 repetitions would be completed with a 2-minute rest between each set. Exercise will begin with 3 pounds weight, but it would be made sure that this wouldn't cause pain during exercise (more than 5/10), gradual progression in weight to 5 pounds after 2nd weeks.

Group A: Tendon neuroplastic training (TNT)

Subjects assigned to this group will undergo static stretching of Extensor carpi radialis brevis and myofascial release for 4 weeks, 3 sessions a week. Myofascial release technique will be applied for 5 minutes and 2 reptations per session

Group B: Conventional treatment

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Both male and female
  • Age between 20-45 years
  • Pain and Tenderness over the lateral epicondyle
  • At least 2 of cozen's test, Maudsley's test and Mill's test will cause pain at lateral epicondylitis.

You may not qualify if:

  • Open wounds
  • Fracture of elbow Humerus, radius, ulna
  • Surgical procedure done around the elbow joint.
  • Elbow instability.
  • Extensor tendon rupture.
  • Symptoms of cervical radiculopathy.
  • Radial nerve entrapment.
  • Major upper limb surgery.
  • Tumor or wound
  • Compartment syndrome of anconeus muscle.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Institute of Rehabilitation Medicine (NIRM)

Islamabad, Capital, 46000, Pakistan

Location

Related Publications (1)

  • Khan H, Razzaq A, Afridi A, Sheraz S, Awan WA. Innovative neuroplastic healing: tendon Neuroplastic Training role in pain alleviation and boosting strength in lateral epicondylitis: a randomized controlled trial. BMC Musculoskelet Disord. 2025 Oct 10;26(1):949. doi: 10.1186/s12891-025-08328-1.

MeSH Terms

Conditions

Tennis Elbow

Condition Hierarchy (Ancestors)

Elbow TendinopathyTendinopathyMuscular DiseasesMusculoskeletal DiseasesElbow InjuriesArm InjuriesWounds and InjuriesTendon Injuries

Study Officials

  • Aisha Razzaq, MSPT-OMPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 22, 2023

First Posted

January 31, 2023

Study Start

January 1, 2023

Primary Completion

February 20, 2023

Study Completion

February 25, 2023

Last Updated

May 6, 2023

Record last verified: 2023-05

Data Sharing

IPD Sharing
Will not share

Locations