- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06302153
Progressive Loading Exercises and Conditioning Exercises on Calf Strain (runners)
Effects of Progressive Loading Exercises and Conditioning Exercises on Pain, Range of Motion and Functions in Calf Strain Among Runners
Study Overview
Status
Intervention / Treatment
Detailed Description
Calf pain is a common complaint among runners of all ages but is most frequent in masters athletes. Calf pain in runners usually results from musculotendinous origins, with the gastrocnemius among the most common of all muscle injuries. The most common calf injury is a tear of the medial gastrocnemius muscle (Tennis Leg) but other structures including the lateral gastrocnemius, plantaris and soleus also may be the cause of muscular pain.There are multiple techniques for the management that involves loading the strained calf musculature through rest, taping techniques, and appropriate soft tissue massage techniques, modalities such as dry needling or western acupuncture can be popular amongst runners and may also be useful. Progressive loading is a principle of resistance training exercise program design that typically relies on increasing load to increase neuromuscular demand to facilitate further adaptations whereas Athletic performance is based on a number of skills that can be developed through a sports conditioning program. This particular program focuses on improving both muscular strength and power using a technique called post-activation potentiation (PAP), also commonly referred to as complex training.
A randomized clinical trial will be conducted at Pakistan sports board, Lahore . Non probability convenience sampling technique will be applied on 40 patients who will be allocated through simple random sampling into group A & group B to collect data. Group A will be given progressive loading exercises and group B will be given conditioning exercises along with stretching. The study will be completed within the time duration of six months. Primary Outcome measures of the research will be pain, range of motion, and functions. Data will be analyzed using SPSS software version 25. After assessing normality of data by Shapiro-wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two groups.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Punjab
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Faisalābad, Punjab, Pakistan, 38000
- Jawad club, Alfatah sports complex
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Faisalābad, Punjab, Pakistan, 5400
- Riphah International University, Raiwind Campus
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Athletes aged 18 years or above
- Pain and tenderness at the back of the lower leg
- self-reported pain ,spasm at back of thigh presenting during sport or at rest (unilateral or bilateral)
Exclusion Criteria:
- Radiating pain or pain with neurogenic and systemic origin
- History of lower limb fracture and surgery
- History of instability at knee or ankle
- Knee or ankle ligamentous or meniscal injury
Study Plan
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: progressive loading exercises
progressive loading exercises Progressive loading exercises & stretching protocol will be given. The exercises included are as follows
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At start of study, a formal educational session, lasting about 30 minutes will be given by the physiotherapist dealing with the treatment/interventions. Whole treatment plan will be given for six weeks.
Pre and post intervention measurements will be taken.
Other Names:
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Experimental: Conditioning Exercises
conditioning exercises Conditioning exercises & stretching protocol will be given. (31)
|
At start of study, a formal educational session, lasting about 30 minutes will be given by the physiotherapist dealing with the treatment/interventions. Whole treatment plan will be given for six weeks.
Pre and post intervention measurements will be taken.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
pain , range of motion, functions
Time Frame: 10 months
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these three variables will be measured during the study
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10 months
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Amna Shahid, MS-DPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- amnashahid
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.
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