- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06905756
Comparative Effect of Accelerated Rehabilitation and Eccentric Strengthening Exercises on Patients With AT
Compartive Effect of Accelerated Rehabilitation and Eccentric Strengthing Exercises on Patient With Achilles Tendinopathy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab
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Lahore, Punjab, Pakistan
- Punjab Social Security Health Management Hospital Manga Raiwind
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male and female patients, age greater than 18 years, clinically diagnosed with Achilles tendinopathy.
- Participants that are clinically diagnosed with Achilles tendinopathy.
- Duration of symptoms or pain for more than 1 month.
- Positive clinical tests, such as Thompson test, confirming Achilles tendinopathy.
- Tenderness to palpation along the Achilles tendon or localized pain during activity.
- Patients with a history of overuse injuries related to repetitive activities, such as running or jumping.
Exclusion Criteria:
- Following participants will be excluded from this study:
- Presence of systemic conditions such as rheumatoid arthritis, diabetes, or other inflammatory or neuromuscular disorders.
- History of complete Achilles tendon rupture or previous surgical intervention on the affected tendon.
- Patients with other lower limb injuries or conditions (e.g., fractures, ligament tears) that could interfere with Achilles tendinopathy treatment.
- Severe tendon degeneration or calcification confirmed by imaging, unsuitable for rehabilitation.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Accelerated rehabilitation
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15 subjects in group A will be receiving Accelerated Rehabilitation protocol alongwith baseline treatment.
Accelerated rehabilitation consisting of three phases, following 12 week exercise regime.
Pain reduction, mobility, strengthening, and functional recovery are part of the accelerated rehabilitation protocol for Achilles tendinopathy.
Ice, TENS, range-of-motion exercises, isometric calf contractions, and a progressive transition to full weight-bearing based are the mainstays of Phase 1 (Weeks 1-4).
Phase 2 (Weeks 5-8) focuses on balance training, resistance band exercises, and seated and standing calf raises as well as light functional workouts like cycling or walking.
Phase 3 (Weeks 9-12) progresses to sport-specific and endurance exercises like swimming or running after including plyometric drills, eccentric heel drops, and advanced strengthening.
Each exercise will be performed under supervision of skilled physiotherapist for 2 times daily, 2 sets of 5 repetitions.
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Experimental: Eccentric strengthening exercises
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Group B will be receiving eccentric strengthening exercises alongwith baseline treatment.
Techniques of Curwin, Stanish et al will be used for eccentric training.
For every exercise, participants do three sets of 15 repetitions, with a 30-second break in between.
Weight is added gradually to enhance resistance (5-10 lbs or more, depending on tolerance).
The eccentric strengthening regimen for Achilles tendinopathy advances every week.
Participants use both feet without dorsiflexion to perform eccentric contractions in Week 1.
By Week 3, the focus of the workouts is on the injured foot in maximum dorsiflexion.
In Week 4, 10% body weight resistance is introduced, and in Week 5, an extra 5-10 pounds.
From Week 6 to Week 8, resistance rises every two weeks.
From Weeks 9 to 12, functional motions like hopping, single-leg heel drops, and sport-specific drills are incorporated, all of which are customized to meet individual goals.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Numerical pain rating scale
Time Frame: 12 Months
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The Pain Scale has a numerical rating system (NRS) with 11 points, with 0 denoting no pain and 10 denoting the most excruciating pain. The following categories apply to scores: 0= denotes no pain 1-3= mild pain 4-6=moderate pain 7-10= severe pain.(12) |
12 Months
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WHOQOL (world health organization and quality of life)
Time Frame: 12 Months
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The WHOQOL uses 26 questions to calculate quality of life across the four domains. Each item is scored on a 5-point Likert scale (1 to 5), where higher scores indicate a better quality of life, lower score indicate, poor quality of life. Average total score for healthy populations is about 90. 0-20 = Poor Quality of Life 21-40 = Moderate Quality of Life 41-60 = Good Quality of Life 61-80 or greater than 80 = Very Good Quality of life. |
12 Months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MSRSW/Batch-Fall23/788
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Achilles Tendinopathy
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Women's College HospitalUniversity Health Network, Toronto; Unity Health Toronto; University of Toronto; The Physicians' Services Incorporated FoundationNot yet recruitingAchilles Tendinopathy | Achilles Insertional TendinopathyCanada
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Cardenal Herrera UniversityCompletedAchilles TendinopathySpain
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Universidad de ZaragozaRecruiting
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-
Riphah International UniversityCompletedEffects of Tissue Flossing on Pain and Functional Performance in Patients With Achilles TendinopathyAchilles Tendinopathy (AT)Pakistan
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Ankara City Hospital BilkentCompletedAchilles Tendinopathy (AT)Turkey (Türkiye)
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