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Effect of Myofacial Release vs. Eccentric Resistance on Pain, ROM and Functional Disability on Achilles Tendonitis

Primary Purpose

Achilles Tendonitis

Status
Completed
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
eccentric resistance exercise
myofascial release
Sponsored by
University of Lahore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Achilles Tendonitis focused on measuring Physiotherapy ,, Myofascial release, Eccentric Resistance, Achilles tendonitis, Pain, Range of motion, Functional Disability

Eligibility Criteria

25 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Both male and female.
  • Age limit 25-50 year.
  • Diagnosed patients by orthopedic surgeon.
  • Achilles tendon symptoms (pain) present in one limb for a minimum of two months.
  • Report having pain rated at least 3 out of 10 on a numerical rating scale (NRS-11).
  • Be able to walk household distances (more than 50 m) without the aid of a walker, crutches or can

Exclusion Criteria:

  • History of Pregnanc.
  • Having history of rheumatoid arthritis or generalized polyarthritis.
  • Pervious history of Achilles tendon rupture or surgery i.e arthrodesis , club foot surgery
  • History of hind foot fracture, or leg-length discrepancy of more than one-half inch.
  • Taken any manual therapy in last 3 month.
  • Contraindication to myofacial releas i.e skin burn or disease

Sites / Locations

  • The University of Lahore

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Myofascial release

eccentric resistance exercise

Arm Description

Group A: This group will receive routine physiotherapy with myofascial release. This protocol will be given for 3 alternative days per week. Each session will be of 45 minutes. Data will be collected at baseline, at 2nd week and at 4th week.

Group B: This group will receive routine physiotherapy and myofascial release with eccentric resistance exercise . This protocol will be given for 3 alternative days per week. Each session will be of 60 minutes. Data will be collected at baseline, at 2nd week and at 4th week.

Outcomes

Primary Outcome Measures

pain intensity
pain intensity will be measured by Numeric Pain Rating Scale
Range of motion
Range of motion will be measured by goniometer
Functional disability
Functional disability will be measured by ankle foot disability index

Secondary Outcome Measures

Full Information

First Posted
September 19, 2022
Last Updated
April 6, 2023
Sponsor
University of Lahore
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1. Study Identification

Unique Protocol Identification Number
NCT05550857
Brief Title
Effect of Myofacial Release vs. Eccentric Resistance on Pain, ROM and Functional Disability on Achilles Tendonitis
Official Title
Comparative Effect of Myofacial Release With and Without Eccentric Resistance on Pain, Range of Motion and Functional Disability in Patients With Achilles Tendonitis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
September 19, 2022 (Actual)
Primary Completion Date
February 28, 2023 (Actual)
Study Completion Date
February 28, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Lahore

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Achilles tendinitis is a common condition that cause pain along back of leg near the heal. It is an overuse injury of the Achilles tendon, the band of tissue that connect calf muscles at the back of the lower leg to heel bone. There are number of treatment approaches to relieve pain in Achilles tendonitis . Insufficient literature has discuss the combine effect of myofascial release with eccentric resistance. So the aim of the study is to compare the effect of myofascial release with eccentric resistance and without eccentric resistance on pain , range of motion and functional disability in patient with Achilles tendinitis
Detailed Description
Tendonitis refers to inflammation of a tendon in response to injury or disease. It causes pain, irritation, and swelling, especially following periods of activity. Achilles tendinitis (AT) is a prevalent condition across the lifespan in both active and sedentary people, and can occur in the mid tendon, tendon insertion to the calcaneus and peritendon. Achilles tendinitis is caused by overuse of the ankle and is closely related to an individuals activity level. In the adult population (21-60 yrs old), the incidence rate is 2.35 persons per 1000. It has been reported in approximately 7%-9% of professional athletes and 6%-18% of regular runners. People with Achilles tendinitis typically report symptoms of pain and stiffness upon weight bearing after prolonged rest and at the start of physical activity, which reduces as the activity continues . These symptoms lead to impaired performance. In more severe cases, pain and disability can be persistent with functional activities such as walking. Physical therapists have used different methods to maintain and also to increase joint motion, and prevent deformity and dysfunction resulting from the muscle shortening. The intension of the physical therapist is to lengthen the musculo-tendinous unit, supporting connective tissue and increase the range of motion. Soft tissue treatments are widely used for AT, but strong scientific evidence to support those treatments is lacking. The literature provides some evidence that heavy pressure and deep massage might have some positive effect on chronic tendonitis by promoting healing. Eccentric training can be effective in the rehabilitation of patients with Achilles tendonitis. The mechanism behind these results is not clear. However, there is evidence that tendons are able to respond to repeated forces by altering their structure and composition, and, thus, their mechanical properties change

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Achilles Tendonitis
Keywords
Physiotherapy ,, Myofascial release, Eccentric Resistance, Achilles tendonitis, Pain, Range of motion, Functional Disability

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
72 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Myofascial release
Arm Type
Active Comparator
Arm Description
Group A: This group will receive routine physiotherapy with myofascial release. This protocol will be given for 3 alternative days per week. Each session will be of 45 minutes. Data will be collected at baseline, at 2nd week and at 4th week.
Arm Title
eccentric resistance exercise
Arm Type
Experimental
Arm Description
Group B: This group will receive routine physiotherapy and myofascial release with eccentric resistance exercise . This protocol will be given for 3 alternative days per week. Each session will be of 60 minutes. Data will be collected at baseline, at 2nd week and at 4th week.
Intervention Type
Other
Intervention Name(s)
eccentric resistance exercise
Intervention Description
The subject will lying prone on a treatment table. One end of eccentric resistance band will tie around the mid of the foot of indvidual, the other end of the resistance band will be attach to the table and the band is adjusted so that it will tight and there will be no slack present in it. It will provide a smooth eccentric resistance throughout the dorsiflexion range
Intervention Type
Other
Intervention Name(s)
myofascial release
Intervention Description
The subject will lye prone on a treatment table. Deep longitudinal massage with the help of both thumbs reinforcing eachother will be given on the subject's calf muscles.
Primary Outcome Measure Information:
Title
pain intensity
Description
pain intensity will be measured by Numeric Pain Rating Scale
Time Frame
change in pain intensity score will be measured at baseline , at 2nd week , at 4th week
Title
Range of motion
Description
Range of motion will be measured by goniometer
Time Frame
Change in range of motion score will be measured at baseline , at 2nd week , at 4th week
Title
Functional disability
Description
Functional disability will be measured by ankle foot disability index
Time Frame
change in Function disability score will be measured at baseline, at 2nd week , at 4th week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Both male and female. Age limit 25-50 year. Diagnosed patients by orthopedic surgeon. Achilles tendon symptoms (pain) present in one limb for a minimum of two months. Report having pain rated at least 3 out of 10 on a numerical rating scale (NRS-11). Be able to walk household distances (more than 50 m) without the aid of a walker, crutches or can Exclusion Criteria: History of Pregnanc. Having history of rheumatoid arthritis or generalized polyarthritis. Pervious history of Achilles tendon rupture or surgery i.e arthrodesis , club foot surgery History of hind foot fracture, or leg-length discrepancy of more than one-half inch. Taken any manual therapy in last 3 month. Contraindication to myofacial releas i.e skin burn or disease
Facility Information:
Facility Name
The University of Lahore
City
Lahore
State/Province
Punjab
ZIP/Postal Code
54000
Country
Pakistan

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Immediately after publication
IPD Sharing Time Frame
Beginning 9 months and ending on 36th month

Learn more about this trial

Effect of Myofacial Release vs. Eccentric Resistance on Pain, ROM and Functional Disability on Achilles Tendonitis

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