Effects of Kinesiotaping and Mulligan Tapping on PFPS

August 10, 2022 updated by: Riphah International University

Comparison of the Effects of Kinesio Taping and Mulligan Taping on Patellofemoral Pain Syndrome.

The aim of this research is to compare the effects of kinesiotaping and mulligan taping on pain, hamstring flexibility, cadence and physical performance of lower limb in patients suffering from patellofemoral pain syndrome according to time duration 24, 48 and 72 hours. Randomized controlled trial done at Riphah International University Rawalpindi campus, Pakistan Railway Hospital and private clinics of twin cities. The sample size was 20. The subjects were divided in two groups, 10 subjects in kinesiotaping group and 10 in mulligan taping group. Study duration was 1 year. Sampling technique applied was non probability convenient sampling technique. Both males and females of 20-35 age bracket having anterior knee pain for more than 2 months and ≥3 pain on NPRS while performing activities i.e. ascending descending stairs, squatting and sitting for extending periods of time were included in study. Tools used in study are NPRS, Kujala pain rating sale, goniometer, active knee extension test, time up and go test.

Study Overview

Detailed Description

Patellofemoral pain syndrome (PFPS) is a frequent musculoskeletal pathology affecting population like adults, teenage boys/girls, military and athletic individuals. It is a probable reason for anterior knee pain in individuals, also known as runner's knee. It is mainly defined as the individuals experience anterior knee pain, including other structural pathology like of patella and retinaculum. There is no related problem of intra articular and peri-patellar impairments. The causes of PFPS includes muscular imbalance of vastus lateralis and vastus medialis, maltracking of patella, instability of hip joint and hind most foot eversion. According to literature the PFPS is mostly common in active young population along with that women are more prone to develop this disease condition as compare to males because of their pelvis anatomy. Wider pelvis area in women causes more stress on knees. The reason of knee joint pain in older people is arthritis (age related degenerative changes). KT tapping has elastic properties like skin, stretching 30 % to 40 % stretching lengthwise. KT has water proof qualities and can be applied for 3 to 5 days. By applying KT over the skin of affected muscle or on joint surface, it reduces the pain, improves the circulation by giving positional impulse through skin, and modify interstitial tissue to reduce skin tension. Mulligan introduced a tapping technique called Mulligan tapping along with Mobilization with Movement technique development. Mulligan tape method prevents the positional malalignment in the joint. Tape may be applied for a week or two and not cause any harm along with mobilization Literature review: Anne Hickey et al. conducted a study in Australia in 2016. In this study effects of mulligan knee tapping technique on pain and lower limb biomechanics was determined. The study concluded that the technique successfully reduced the knee pain, decreased hip internal rotation and active gluteal muscles earlier. Leticia Lopes Aguiar et al. conducted a study in which he determines the effect of mulligan concept among ballet dancers. The study concluded that mulligan concept had significant results to improve pain threshold. Samara Alencar Melo et al. in which KT taping effects was determined on pain and muscular performance in patellofemoral pain syndrome patients did a study in 2018. In this RCT, the results showed that KT causes reduction in pain within 72 hours after its application without causing tension around skin. In 2017, Neelam Rehman et al. in Pakistan conducted a study. In this research the immediate effects of KT on pain in athletic population having PFPS was determined. The study concluded that KT had immediate effects in reducing pain and it can be used to treat immediate post injuries in athletic population.

Study Type

Interventional

Enrollment (Actual)

20

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

    • Punjab
      • Rawalpindi, Punjab, Pakistan, 46000
        • Riphah Rehabilitation Center

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

20 years to 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Anterior knee pain which is persisting longer than two months (pain on ascending and/or descending stairs, squatting, sitting for extended periods of time).
  • Pain scoring rate on NPRS scale three or more during at least two activities.
  • Age between 20 and 35 years.
  • Both Male and female.

Exclusion Criteria:

  • Meniscus tears, bursitis, patellar tendon, any ligamentous injury, any joint degeneration changes and patellofemoral dislocation and/or frequent subluxation.
  • Undergone lower extremity surgery
  • Patients having knee pain due to hip, lumbar spine and ankle joints
  • Dermatitis and any other skin problem

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: group 1
This group receives KinesioTaping along with conventional treatment

Kinesio-taping with conventional therapy 24, 48 and 72 hours standardized therapeutic KT application along with conventional therapy (hot pack, strengthening and stretching exercises). The patient laid supine.To maintain proprioceptive stimulation in the quadriceps (from origin towards insertion) and to alleviate the tension of hamstring muscle, a 'Y'-shaped kinesiotaping will be applied. Afterward, 2 pieces of 'I'-shaped tapes were stretched by 75% through the mechanical correction technique and will be applied around the patellar circumference in the way that it would allow the patella to move naturally in the femoral cavity while the knee was in 45 flexion

CONVENTIONAL THERAPY:

Stretching of hamstrings 10 reps 10 sec hold. Straight leg raise 3 sets* 10 reps, 1 min interval. Strengthening of Quadriceps (quads isometric) and VMO with 10 reps and 3 sets, 1 min interval) Squatting (10 reps* 3 sets, 1 min interval)

Experimental: group 2
This group receives mulligan taping along with conventional treatment

Mulligan taping will be applied while patient in standing position and the hip, knee will be internally rotated and flexed to 20 degree. Rigid tape will be applied from neck of fibula which will be passing anteriorly over the tibia to secure internal rotation of tibia at the knee, and passing below the medial joint line and behind the knee, 2 superimposed layers of 38-mm rigid tape will be applied in a spiral fashion. Tape will be applied for 24, 48 and 72 hours. And it must come off immediately if any pain and skin irritation is experienced. Along with conventional therapy.

Stretching of hamstrings 10 reps 10 sec hold. Straight leg raise 3 sets* 10 reps, 1 min interval. Strengthening of Quadriceps (quads isometric) and VMO with 10 reps and 3 sets, 1 min interval) Squatting (10 reps* 3 sets, 1 min interval)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Kujala pain Rating score
Time Frame: 72 hours
The Kujala pain rating scale is a 13-item screening instrument designed to assess patellofemoral pain in adolescents and young adults, with a variable ordinal response format. For example, a 'Limp' score would be scored as follows: none (5), slight/periodic (3), constant (0). Total scores range from 0 to 100.
72 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numeric pain rating scale
Time Frame: 72 hours
Numeric pain rating scale is used to assess the intensity of pain before and after intervention. Its value ranges from 0-10. O indicates no pain and 10 indicate maximum pain. Reliability of this tool is r=0.957. It will be measured at 24 hour, 48 hour, and 72 hour.
72 hours
Time Up and Go
Time Frame: 72 hours
Time up and go test is used to assess the dynamic balance ability, in this subject took to rise from 46cm height arm chair, walk 3 meter, turn back at affected side and walk back to chair and sit. Reliability of this tool is r = 0.98 to 0.99. It will be measured at 24 hour, 48 hour, and 72 hour
72 hours
Active Knee Extension Test
Time Frame: 72 hours
To check hamstring flexibility, patient position is in supine and effected leg is in 90-degree hip flexion. Patient is asked to extend the knee. The actual cutoff value for the Active knee extension test is 160. Normal individual has range of >160 or equal to160 (=160) and angle <160 considered hamstring tightness.)
72 hours

Collaborators and Investigators

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

November 15, 2021

Primary Completion (Actual)

April 30, 2022

Study Completion (Actual)

May 15, 2022

Study Registration Dates

First Submitted

November 8, 2021

First Submitted That Met QC Criteria

November 8, 2021

First Posted (Actual)

November 18, 2021

Study Record Updates

Last Update Posted (Actual)

August 11, 2022

Last Update Submitted That Met QC Criteria

August 10, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

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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