- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05736809
Calcaneal Low Dye Taping Plantar Fascial Stretching and Sham Taping in Football Players
February 20, 2023 updated by: Riphah International University
Comparative Effects of Calcaneal Low Dye Taping Plantar Fascial Stretching and Sham Taping on Acute Plantar Heal Pain and Functional Activity Level in Football Players
Showing the effect of calcaneal Low-dye Taping on acute planter heel pain and functional activity level in football players.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
Planter fascia is a fibrous connective tissue originate from the medial calcaneal tubercle and help support the arch of the foot repetitive tensile overload from standing for long periods of time or running causes changes in the aponeurosis.
Patient mostly present with pain on first step in the morning or after long non-weight bearing , Tenderness to anterior medial head.
Its can first be treated conservatively where 90 % cases treated greater then 6 months of duration.
Baseline treatment is given as Rest , Ice , compression and Elevation , with this NSAID ,shoe inset ,Taping, orthotics, deep friction massage and precautions are advised to the patients.
Arch taping is most probably used and orthotics in acute treatment is commonly preferred due to its cost.Taping effects most probably overlooked in general gait parameters, patient feedback on pain relief and function recovery.
Study Type
Interventional
Enrollment (Actual)
21
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
-
Lahore, Punjab, Pakistan, 54000
- Surya Azeem Hospital
-
-
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 45 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Both male and female football players
- Age (20-45 yrs)
- Pain with the first step upon walking
- Pain located at the heel or Planter surface of Mid-foot consistent with Planter fasciitis
- Presence of an everted calcaneus greater than or equal to 2°
Exclusion Criteria:
- Patient with surgery and treatment with previous 6 month
- History of Ankle or foot fracture
- Congenital deformity of the foot and ankle
- Sever Spasticity
- Use of an Assistive device
- Bilateral Planter heel pain
- Refusal to participate in study
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: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Low-Dye taping
out of 21 participants 7 will be included in the study design as an experimental group using low-dye taping in acute stage
|
Low-dye taing using 4 tapes around calcaneam
|
|
Active Comparator: Plantar fascia stretching
out of 21 participants 7 will be included in the study design as an active participants group using plantar fscia stretching in acute stage
|
out of 21 participants 7 will be included in the study design as an active participants group using plantar fscia stretching in acute stage
|
|
Placebo Comparator: Sham taping
out of 21 participants 7 will be included in the study design as an active participants group using plantar fscia stretching in acute stage
|
out of 21 participants 7 will be included in the study design as an plecebo group using sham taping in acute stage
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
numeric pain rating scale
Time Frame: 3 week
|
The Numeric Pain Rating Scale (NPRS) is a famous strategy to evaluate Pain.
The NPRS has a dependable, substantial and delicate instrument to survey torment.
Torment score as per the NPRS (0-10), made during the principal strides toward the beginning of the day, was the essential result (0 as "no aggravation" and 10 as "exceptionally serious agony").
|
3 week
|
|
foot and ankle disability index
Time Frame: 3 week
|
It is utilized to evaluate the utilitarian restrictions connected with foot and lower leg, action of day to day living and most troublesome errand that are vital for sports e.g., Walk, word related execution, Agony, Rest and Strength.
The foot and ankle disability index (FADI) is scored out of 104, with a score of 0 indicating maximum disability and a score of 104 indicating no disability.
The total FADI score corresponds to the sum of Activity and Pain subscale scores (maximum score of 88 for Activity and 16 for Pain).
|
3 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Fatima Dr Tariq, Phd, Riphah International University
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)
December 19, 2022
Primary Completion (Anticipated)
February 1, 2023
Study Completion (Anticipated)
February 1, 2023
Study Registration Dates
First Submitted
January 4, 2023
First Submitted That Met QC Criteria
February 20, 2023
First Posted (Estimate)
February 21, 2023
Study Record Updates
Last Update Posted (Estimate)
February 21, 2023
Last Update Submitted That Met QC Criteria
February 20, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 30162
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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