Foundation University College of Physical Thrapy
Islamabad, 44000, Pakistan
Location status: Recruiting
NCT Number: NCT06674057
A randomized control trial will be done on diagnosed stroke patients of subacute stage in Fauji Foundation Hospital Rawalpindi and leading edge physical therapy and rehabilitation clinic.The purpose of the study is to determine Additional Effects of Kinesio-Taping along with conservative Physical Therapy on upper limb function, Range of motion and Spasticity in the patients with Subacute Stroke. The conservational physical therapy includes Passive and active ROMs 25 repetitions each, 3 times per week. PNF stretching (hold relax) for spastic muscles for 20 repetitions with a 10 second hold and 10 second relaxation of the muscle group 3 times per week.
D1 flexion and extension for 20 repetitions 3 times per week. Kinesio tape 3 times per week. (Anchor opposed to effected compartment to provide facilitation and sustained stretch). with srtrngth training included in week 3-6 with a resistance band of medium resistance.
treatment time will be 30 minutes on alternate days for six weeks.
Interested in participating?
Request Info40 year–65 year
All sexes
Interventional
Not applicable
Islamabad, 44000, Pakistan
Location status: Recruiting
OBJECTIVES:
The objectives of this study are:
HYPOTHESIS:
Alternate Hypothesis:
There is a statistically significant difference between kinesio taping combined with physical therapy on ROM, spacticity and function of upper limb Shoulder, elbow and wrist joints in patients with subacute stroke compared to conventional physical therapy.
Null Hypothesis:
There is no statistically significant difference between kinesio taping combined with physical therapy on ROM, spacticity and function of upper limb Shoulder, elbow and wrist joints in patients with subacute stroke compared to conventional physical therapy.
Research Design: Experimental study. Randomized Control Trial
Clinical setting: Rehabilitation department, Fauji Foundation Hospital , leading edge physical therapy and rehabilitation islamabad.
Study duration: 6 months.
Selection Criteria:
Inclusion criteria
Exclusion criteria
Sampling technique: Convenience sampling
Outcome Measures:
Data will be collected on Demographics and general information Goniometer will be used to assess the range of motion of shoulder, elbow and wrist joint Modified Ashworth scale will be used to determine the level of spasticity in the participants.
Wolf motor function test scale for upper limb will be used to assess upper limb function.
Experimental Group (A) = This group will receive kinesio taping every alternate day for six weeks combined with conservational physical therapy which includes AROMs, PROMs, PNF D1 flexion and extension, resistance raining using resistance band of medium resistane.
and their outcomes will be measured at baseline and at 3rd week and at the end of 6th week treatment.
Control group (B) =this group will not receieve kinesio taping , only conservationall Physical therapy will be given and their outcomes will be observed at the baseline, at third week and then after treatment of 06 weeks.
Data analysis techniques:
The data will be analyzed through SPSS 21 and Data would be analyzed based on the study design chosen that is random control experimental study.
A printed questionnaire will be provided to the participents after obtaining written consent and providing adequate explanation regarding the study, after which the data will be presented in the form of graphs or tables.
Significance of the study:
This study will add data to the literature. Providing evidence-based data and aiding healthcare providers to incorporate kinesio taping as an adjunct intervention.
This study will also provide a feasible and cost-effective treatment to the patient diagnosed with subacute stroke.
Kinesio taping is easy to apply, potentially beneficial treatment options for patients with subacute stroke upper limb dysfunction.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The experimental group will receive the following treatment for week 1-3 (3 days on alternate days):
For week 3-6 the treatment will include:
The control group will receive the following treatment for week 1-3 on alternate days:
For week 3-6 the treatment will include:
Time frame: 6 weeks
velocity dependant passive resistance to stretch will be assesed using the modified ashworth scale.
Time frame: 6 weeks
Upper limb function will be assessed using the wolf motor function test for upper limb.
Time frame: 6 weeks
range of motion of Wrist, Elbow and shoulder joint will be assessed using a goiniometer.
Contact information is provided by the study sponsor or research team.
Foundation University Islamabad
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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