Protocol summary

Study aim
patellofemoral pain syndrome
Design
randomized clinical trial
Settings and conduct
district headquarter hospital Jhang and Iqbal memorial hospital Jhang
Participants/Inclusion and exclusion criteria
Inclusion criteria: • 18-40 years adults having PFP for more than three months • PFP bring forth during clinical examination (patellar grind test, apprehension test) • PFP in at least two functional activities (sitting for long time, stairs climbing, running, squatting, kneeling and jumping) • Both male & female • Patients with moderate pain ranging from 3 to 7 Exclusion criteria: • Any lower limb surgery in past 6 months • History of dislocation or subluxation of patella in past 6 months • Allergy from taping • Chronic illness that may limit training • Knee osteoarthritis (patellofemoral and tibiofemoral joint) • Chondromalacia patellae • Pes anserine bursitis
Intervention groups
two groups(group A & group B): both groups get 12 session with alternate days in 4 weeks.
Main outcome variables
visual analogue scale and Anterior Knee Pain Scale

General information

Reason for update
Acronym
IRCT registration information
IRCT registration number: IRCT20220520054932N1
Registration date: 2022-05-27, 1401/03/06
Registration timing: retrospective

Last update: 2022-05-27, 1401/03/06
Update count: 0
Registration date
2022-05-27, 1401/03/06
Registrant information
Name
Hafiza Kinza Shakoor
Name of organization / entity
The University of Faisalabad
Country
Pakistan
Phone
+92 309 1106072
Email address
mspp-fa20-030@tuf.edu.pk
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2022-03-20, 1400/12/29
Expected recruitment end date
2022-03-28, 1401/01/08
Actual recruitment start date
empty
Actual recruitment end date
empty
Trial completion date
empty
Scientific title
EFFECT OF MULLIGAN’S PAIN RELEASE PHENOMENON ALONG WITH KINESIOTAPING IN PATELLOFEMORAL PAIN SYNDROME
Public title
EFFECT OF MULLIGAN’S PAIN RELEASE PHENOMENON ALONG WITH KINESIOTAPING IN PATELLOFEMORAL PAIN SYNDROME
Purpose
Treatment
Inclusion/Exclusion criteria
Inclusion criteria:
• 18-40 years adults having PFP for more than three months • PFP bring forth during clinical examination (patellar grind test, apprehension test) • PFP in at least two functional activities (sitting for long time, stairs climbing, running, squatting, kneeling and jumping) • Both male & female • Patients with moderate pain ranging from 3 to 7
Exclusion criteria:
• Any lower limb surgery in past 6 months • History of dislocation or subluxation of patella in past 6 months • Allergy from taping • Chronic illness that may limit training • Knee osteoarthritis (patellofemoral and tibiofemoral joint) • Chondromalacia patellae • Pes anserine bursitis (2)
Age
From 18 years old to 40 years old
Gender
Both
Phase
N/A
Groups that have been masked
  • Participant
Sample size
Target sample size: 40
Randomization (investigator's opinion)
Randomized
Randomization description
patients that fulfill the inclusion criteria will be randomly divided into experimental and active control group by using the lottery method
Blinding (investigator's opinion)
Single blinded
Blinding description
participant is blinded means they do not know what treatment the other group gets.
Placebo
Not used
Assignment
Parallel
Other design features

Secondary Ids

empty

Ethics committees

1

Ethics committee
Name of ethics committee
Ethics committee of the university of Faisalabad
Street address
house#560,Mohalla sheikh lahory
City
Jhang Sadar
Postal code
35200
Approval date
2022-03-13, 1400/12/22
Ethics committee reference number
1021

Health conditions studied

1

Description of health condition studied
Patellofemoral pain syndrome
ICD-10 code
ICD-10 code description

Primary outcomes

1

Description
pain
Timepoint
total 4 weeks of interventional period with alternate days contain 12 sessions. visual analogue scale will be used before and after completion of treatment session
Method of measurement
visual analogue scale

Secondary outcomes

1

Description
Anterior knee pain
Timepoint
total 4 weeks of interventional period with alternate days contain 12 sessions. Anterior Knee Pain scale will be used before and after completion of treatment session
Method of measurement
Anterior Knee Pain scale

Intervention groups

1

Description
Intervention group: 1, this group will receive Mulligan's pain release phenomenon and baseline treatment(kinesiotaping, strengthening of vastus medialis oblique muscle and Ultrasonic) in12 sessions for 4 weeks with alternate days. compression PRP will be provided by compressing patella against condyles of femur then knee joint will be moved in flexion and extension while maintaining the compression for 15 seconds. visual analogue scale and Anterior Knee Pain scale will be used to get reading before and after the completion of treatment sessions
Category
Rehabilitation

2

Description
Active Control group: Group B will be given Baseline treatment which includes Kinesiotaping of patellofemoral joint and strengthening of Vastus medialis Oblique muscle and Ultrasonic. in12 sessions for 4 weeks with alternate days.visual analogue scale and Anterior Knee Pain scale will be used to get reading before and after the completion of treatment sessions
Category
Rehabilitation

Recruitment centers

1

Recruitment center
Name of recruitment center
DHQ Hospital Jhang
Full name of responsible person
Dr Riffat Amar
Street address
house # 560, Mohalla Sheikh Lahory
City
Jhang
Postal code
35200
Phone
+92 309 1106072
Email
hafizakinzashakoor567@yahoo.com

Sponsors / Funding sources

1

Sponsor
Name of organization / entity
The University of Faisalabad
Full name of responsible person
Dr Sidra Majeed
Street address
house # 560,Mohalla Sheikh Lahory
City
Jhang Sadar
Postal code
35200
Phone
+92 309 1106072
Email
hafizakinzashakoor567@yahoo.com
Grant name
Grant code / Reference number
Is the source of funding the same sponsor organization/entity?
Yes
Title of funding source
The University of Faisalabad
Proportion provided by this source
100
Public or private sector
Private
Domestic or foreign origin
Foreign
Category of foreign source of funding
Sponsor: country of origin
Country of origin
Pa
Type of organization providing the funding
Academic

Person responsible for general inquiries

Contact
Name of organization / entity
The University of Faisalabad
Full name of responsible person
Dr Sidra Majeed
Position
Assistant Professor
Latest degree
Master
Other areas of specialty/work
Physiotherapy
Street address
house #560, Mohalla sheikh lahory
City
Jhang Sadar
Province
Punjab
Postal code
35200
Phone
+92 309 1106072
Email
hafizakinzashakoor567@yahoo.com

Person responsible for scientific inquiries

Contact
Name of organization / entity
The University of Faisalabad
Full name of responsible person
Dr Sidra Majeed
Position
Assistant Professor
Latest degree
Master
Other areas of specialty/work
Physiotherapy
Street address
House # 560, Mohalla sheikh lahory
City
Jhang Sadar
Province
Punjab
Postal code
35200
Phone
+92 309 1106072
Email
hafizakinzashakoor567@yahoo.com

Person responsible for updating data

Contact
Name of organization / entity
Private clinic
Full name of responsible person
Dr Hafiza Kinza Shakoor
Position
clinical Physiotherapist
Latest degree
Master
Other areas of specialty/work
Physiotherapy
Street address
house # 560, Mohalla sheikh lahory
City
Jhang Sadar
Province
Punjab
Postal code
35200
Phone
+92 309 1106072
Email
hafizakinzashakoor567@yahoo.com

Sharing plan

Deidentified Individual Participant Data Set (IPD)
Yes - There is a plan to make this available
Study Protocol
Yes - There is a plan to make this available
Statistical Analysis Plan
Yes - There is a plan to make this available
Informed Consent Form
Yes - There is a plan to make this available
Clinical Study Report
Yes - There is a plan to make this available
Analytic Code
No - There is not a plan to make this available
Data Dictionary
No - There is not a plan to make this available
Title and more details about the data/document
IPD collected for primary and secondary outcome measures
When the data will become available and for how long
Jan 2023
To whom data/document is available
people working in any domain can be authorized to get this data
Under which criteria data/document could be used
Any wrong information or editional errors
From where data/document is obtainable
this data is only available on-demand via email mention to the person responsible
What processes are involved for a request to access data/document
documents can also be processed via university emails
Comments
Data is private legacy respect it
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