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Patellofemoral Pain SyndromeNCT06598618

Comparison of IASTM and Muscle Energy Technique in Patellofemoral Pain Syndrome.

A study testing Graston technique+ Conventional PT and Muscle energy technique + Conventional PT in people with Patellofemoral Pain Syndrome, run by Riphah International University at 1 site in Pakistan.

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Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The aim of this randomized controlled trial is to compare the effect of Instrument Assisted Soft Tissue Mobilization (IASTM) and muscle energy technique on iliotibial band tightness on pain, range of motion and functional mobility in patients with patellofemoral pain syndrome. Read more about this study

Who is it for?
Ages 18 to 35 years
Conditions the study is for
Patellofemoral Pain Syndrome
What is being tested?
Graston technique+ Conventional PT and Muscle energy technique + Conventional PT
Could I receive a placebo?
No, everyone receives an active treatment
How many people
48 participants
Where
1 sitePakistan
Study dates
2 Oct 2024to 28 Sep 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • • Age between 18 and 35 years
  • Both Genders.
  • Anterior or retro patellar knee pain for at least the past 3 months.
  • Knee pain during at least 3 of the following activities: ascending/descending stairs, squatting, hopping/ running, and prolonged sitting.
  • Retro patellar pain in patellar grind test (positive clarke's sign).
  • A score of at least 3 on the visual analog scale (VAS).
  • Positive Ober's test.

Who cannot join

  • • Any meniscal or ligament tears of knee.
  • Knee osteoarthritis.
  • Any previous surgery of lower limb.
  • Patellar fracture or fracture of lower extremity.
  • Having received knee injections of corticosteroids or hyaluronic acid.
  • Osteoporosis of knee joint.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

KINZA ANWAR, MS-OMPT contact

+92-3239735427

kinza.anwar@riphah.edu.pk

Pakistan1 site, 1 recruiting
  • Pakistan Railway hospital

    Rawalpindi, Punjab Province, 46600

    KINZA ANWAR, MS-OMPT, +92-3239735427, kinza.anwar@riphah.edu.pk

    ALEEZAE SHAMIM, MS-OMPT*

    Recruiting

Other trials in Pakistan

About this study

Official title: Compare the Effects of Instrument Assisted Soft Tissue Mobilization (IASTM) and Muscle Energy Technique on Iliotibial Band Tightness in Patients With Patellofemoral Syndrome.

The aim of this randomized controlled trial is to compare the effect of Instrument Assisted Soft Tissue Mobilization (IASTM) and muscle energy technique on iliotibial band tightness on pain, range of motion and functional mobility in patients with patellofemoral pain syndrome.

Read the detailed description

Patellofemoral pain syndrome (PFPS) is termed as anterior knee pain and is characterized by peripatellar or retro patellar pain as a result of changes in the physical and biochemical components of the patellofemoral joint due to increased load during activities such as running, squatting, going up and down stairs, cycling and jumping. Patellofemoral syndrome is one of the most common knee conditions seen by clinicians. In active individuals, it may account for 25% to 40% of all knee problems The iliotibial band is a lateral thickening of the fascia which attaches to the tensor fascia lata proximally. Most of the lateral retinaculum (superficial oblique and deep transverse portion) arises from the ITB, therefore the ITB indirectly provides lateral stabilisation and acts as a passive restraint to medial patella glide. A tight ITB could theoretically lead to lateral patella tracking, lateral patella tilt and lateral patella compression. Several authors have suggested that tightness in the iliotibial band may contribute to patellofemoral syndrome and knee pain by pulling the patella laterally, thereby causing abnormal tracking of the patella in the trochlear groove.

The Instrument-Assisted Soft Tissue Mobilization (IASTM) technique is the most frequent soft tissue mobilization techniques. It involves the use of a tool that causes mechanical micro-traumatic injury to the treated area. As a result, an inflammatory reaction is elicited, speeding up the healing process and restoring the flexibility and integrity of the tissue and cartilage healing. The therapeutic effects of this approach appear to include decreasing tissue adhesion, enhancing the number of fibroblasts, and stimulating collagen synthesis.

Muscle energy technique is a soft tissue technique designed to improve musculoskeletal function through stretching tight muscles and fascia, to reduce pain and improve circulation. MET is characterized by a patient-induced skeletal muscle contraction against physiotherapist resistance in a controlled direction and position. The pathological barrier of a muscle is located through joint positioning which is followed by active muscle contraction by the patient moving away from the resistance followed by relaxation of the muscle. A new pathological barrier is located through passive movement and the process is repeated.

The rationale for the use of these techniques is to compare the effects of IASTM and MET of iliotibial band tightness in improving pain, range of motion and functional mobility in patients with patellofemoral pain syndrome.

Being tested
Graston technique+ Conventional PT, Muscle energy technique + Conventional PT
Keywords
IASTM, MET, iliotibial band, patellofemoral pain syndrome
Medical subject headings
Patellofemoral Pain Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Graston technique+ Conventional PTOther

    IASTM technique (graston technique) on iliotibial band. Frequency 2 sessions of stroking with 20 seconds rest in between 3 times/week for 3 consecutive weeks Intensity as tolerated by patient. Conventional PT including 1- Therapeutic ultrasound at frequency of 3.5 MHZ for 10 minutes. 2- Stretching exercise of hamstrings. 3-Isometric exercises of Quadriceps

  • Muscle energy technique + Conventional PTOther

    Muscle energy technique (post facilitation stretch) on iliotibial band. Frequency 10 repetitions 3 times/week for 3 consecutive weeks Intensity starting from 50 percent resistance across barrier provided by physiotherapist.. Conventional PT including 1- Therapeutic ultrasound at frequency of 3.5 MHZ for 10 minutes. 2- Stretching exercise of hamstrings. 3-Isometric exercises of Quadriceps.

Study groups in NCT06598618
Study groupRoleWhat they receive
Graston technique+ Conventional PTActive comparatorNot described
Receives: Other: Graston technique+ Conventional PT
Muscle energy technique + Conventional PTOtherNot described
Receives: Other: Muscle energy technique + Conventional PT

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Visual analogue scale (VAS)

    The VAS is a reliable, valid, responsive, and frequently used pain outcome measure. It consists of a bidirectional 10 cm straight line with two labels, that is, "no pain" and "worst possible pain", located at either end of the line.

    VAS consists of a bidirectional 10 cm straight line with two labels, that is, "no pain" and "worst possible pain", located at either end of the line. Patients are instructed to draw a vertical mark on the line indicating their pain level.

    Measured: 3 weeks

  2. Goniometer

    A goniometer is an instrument that measures the available range of motion at a joint.

    Measured: 3 weeks

  3. Kujala questionnaire

    The Kujala AKPS is a 13-item screening instrument designed to assess Patellofemoral pain in adolescents and young adults. The total score of the questionnaire is equal to 100, which shows the maximum function of the knee joint.

    Measured: 3 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Sep 2024
  2. Study start2 Oct 2024
  3. Primary completion25 Sep 2025 (estimated)
  4. Study completion28 Sep 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
48 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06598618
Sponsor's protocol ID
REC/01872 Aleezae Shamim
Status last verified
Feb 2025
First submitted
12 Sep 2024
Last updated
21 Feb 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Graston technique+ Conventional PT and Muscle energy technique + Conventional PT in people with Patellofemoral Pain Syndrome, run by Riphah International University at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 21 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact KINZA ANWAR, MS-OMPT (+92-3239735427, kinza.anwar@riphah.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Visual analogue scale (VAS) (time frame: 3 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Feb 2025.

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