Foundation University College of Physical Therapy
Islamabad, 44000, Pakistan
NCT Number: NCT06947239
The estimated annual incidence of stroke in Pakistan is 250/100, 000. Upper limb impairments and post-stroke musculoskeletal complications such as pain, subluxation and restricted joint range of motion are commonly reported. Among many other shoulder impairments, adhesive capsulitis is a leading cause of limited mobility, reduced range of motion, and pain in stroke patients.
The aim of the current study will benefit the clinicians and physiotherapists as it provide an insight to treat post stroke adhesive capsulitis. Effects of mirror therapy have been established but the literature does not provide best treatment approaches or modalities for different types of Hemiplegic shoulder pain. This study will address the limitations in treatment approaches concerning the shoulder joint and its mobility in post-stroke adhesive capsulitis.
The study will be non-blinded randomized control trial, consisting of two groups. Study will be conducted over a period of 1 year. Subjects will be selected via non-probability purposive sampling technique using coin toss method followed by randomization into two groups (A and B).Ethical approval will be obtained from ERC FUMC.
One group will receive mirror therapy while other will receive conventional exercises treatment for period of 6 weeks. Baseline tests will be performed before and after the intervention of mirror therapy & outcome measure assessments will be done after every 3 weeks for a total period of 6 weeks intervention period. Data will be entered and analyzed on SPSS version 22.
Looking for future studies?
Notify Me40 year–70 year
All sexes
Interventional
Not applicable
Islamabad, 44000, Pakistan
OBJECTIVES OF STUDY
HYPOTHESIS ALTERNATE HYPOTHESIS
NULL HYPOTHESIS
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The experimental group will receive 20 minutes of conventional therapy followed by 20 minutes of mirror therapy training including 3 minutes of rest period between the interventions.
WEEK OF INTERVENTION:
TASK PERFORM IN FRONT OF MIRROR:
WEEK :1-2
ACTIVE SHOULDER ROM:
flexion, abduction, external-internal rotation movements of the intact extremity
Increase the number of repetition according to the patient progression
WEEK:3-4
ACTIVITIES TARGETING SHOULDER ROM:
Cleaning the mirror with a towel(internal rotation+ abduction)
Lifting a glass to drink ( flexion + abduction)
Holding a brush to comb hair (external rotation
WEEK:5-6
Overhead reaching
(pasting stickers on the
mirror)(internal rotation
/ abduction)
Lifting a bottle overhead.
( flexion/abduction)
Throwing a ball (external
rotation)
PROGRESSION OF TASK SPECIFIC MIRROR THERAPY:
WEEK: 1-2 Increase the number of repetition according to the patient progression WEEK:3-4 Add water in glass Transfer glass
Details: Weeks wise:
The control group will receive 20 mints of conventional therapy .
Time frame: 6 weeks
Goniometer will be used to assess range of motion at the shoulder
Time frame: 6 weeks
Montreal cognitive assessment test that was used to detect mild cognitive impairment
Foundation University Islamabad
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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.
Published trials that share one or more normalized conditions with this study.
NCT07648732
Nervous System Diseases, Neurologic Manifestations
View Trial DetailsNCT07598812
Back Pain, Exercise Training
Alexandria, Alexandria Governorate, Egypt
View Trial DetailsNCT06374862
Muscle Strength, Musculoskeletal Manipulations
Amiens, Picardie, France
View Trial DetailsNCT07367334
Breast Cancer Survivors, Cortisol
Chennai, Tamil Nadu, India
View Trial Details