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It will be a randomized control trial with 112 patients which will be divided into two groups of 56 patients in each group. Participants will recruit through convenient sampling techniques.
Outcome measures are range of motion and spasticity. The protocol was implemented three days per week for eight consecutive weeks. Data will be collected at baseline and 8 th week after intervention.
Full description
Objective of the study is to compare the effects of the agonist contract-relax technique versus the antagonist contract-relax technique on spasticity and range of motion in individuals with chronic stroke.
Null hypothesis (H0):
There are no comparative effects of agonist contact-relax technique and the antagonist contract-relax technique on spasticity and ankle range of motion in chronic patients.
The alternate hypothesis (HA):
There are comparative effects of agonist contract-relax technique and the antagonist contract-relax technique on spasticity and ankle range of motion in chronic stroke patients.
The sample size came out to 94 (47 in each group) after adding 20% dropout the sample size was 47+9=56 in each group.
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Interventional model
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112 participants in 2 patient groups
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Central trial contact
momna Asghar, MPTN
Data sourced from clinicaltrials.gov
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