- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06807814
COMPERATIVE EFFECTS of CONSTRAINT- INDUCED MOVEMENT THERAPY and MIRROR THERAPY on FUNCTIONAL AMBULATION and QUALITY of LIFE in CHRONIC STROKE PATIENTS
Stroke is a global health issue as this happens when the blood flow to the brain is disrupted or reduced, depriving the brain tissue of sugar and oxygen. This interruption affects the brain cells hence leading to the loss of a cell Various physical, cognitive and emotional losses are experienced. Cerebrovascular accident or simply stroke, is the fifth cause of mortality and one of the most common causes of disability in the United States of America (Campbell et al., 2019). There are two main types of stroke: ischemic and hemorrhagic. An ischemic stroke is characterized by an occlusion of a cerebral artery by an embolus or thrombus while hemorrhagic stroke results from a hemorrhage in the brain due to rupture of a blood vessel. A TIA or so-called mini stroke occurs when the clot is not severe enough to result in lasting symptoms (Feigin et al., 2022; Strilciuc et al., 2023).
Strokes substantially affect an individual mobility and overall quality of life, although few comparative studies comparing CIMT and MT exist in the literature. This research therefore seeks to systematically compare the effects of these two interventions on functional ambulation and quality of life of chronic stroke patients. Hereby, the research compares structured, task specific CIMT with the less structured, more general approach of MT in order to offer clinicians empirically founded recommendations on what course of action might prove effective for patients. This study also provides new insights to the field given that it not only describes the potential of CIMT within outpatient physiotherapy treatment but also provides an overview of the long-term effects for patients with stroke. These outcomes of this study will be useful in developing rehabilitative research, improving clinical practice protocols, and thereby improve the lifestyles of people living with chronic stroke.
Study Overview
Status
Intervention / Treatment
Detailed Description
To compare the effects of MT and CIMT on functional ambulation and quality of life in chronic stroke patients.
Study Design: This was a randomized controlled trial with two parallel groups:
Group A (Constraint-Induced Movement Therapy (CIMT)):
A well-defined and structured rehabilitation program that restricts the use of the unaffected limb to promote the functional recovery of the affected limb in chronic stroke patients(Franck et al., 2019).
- Group B (Mirror Therapy):
A specific intervention that uses a mirror to create a visual illusion of the affected limb, with the goal of improving motor function and quality of life in chronic stroke patients
- Screening: Patients was screened to meet inclusion criteria. The consent form was taken from patients then patients was randomly allocated into two groups (33 in each group).
- Randomization: Patients fulfilling the inclusion criteria will be randomly divided into experimental and control groups using the computer software.
- Blinding: The study will be single blinded. The assessor, who has 5 years of experience in both clinical practice and research, will be unaware of the treatment given to both groups and will assess the participants objectively.
- Allocation: Allocation of the participants will be concealed, and envelope concealment method will be used for it.
- Outcome Measures:
- Functional Ambulation Categories (FAC)
- Tinetti gait and balance score (POMA)
- Short Form Health Survey (SF-12) Ethical Considerations: This study has received ethical approval from the Institutional Review Board (IRB). Informed consent was obtained from all participants.
Data Analysis: Statistical software was used to analyze the data, with appropriate tests employed based on data normality to compare outcomes between groups.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 5654590
- University of Lahore Teaching Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants having age between 21 and 70 years old were recruited (e Silva et al., 2017).
Both genders included (e Silva et al., 2017).
- Diagnosed with post chronic hemiplegia ischemic stroke (≥6 months) affecting one side of the body(Danlami & Abdullahi, 2017; Mansfield et al., 2018).
- Participants having ability to follow verbal and visual instructions(Danlami & Abdullahi, 2017).
- Participants having no significant cognitive impairment (Minimental state examination score ≥ 17(Danlami & Abdullahi, 2017).
- Participants having low risk of fall (Tinetti gait and balance score ≥20)(Danlami & Abdullahi, 2017).
Exclusion Criteria:
- History of other neurological conditions affecting mobility. (Mansfield et al., 2018).
Unstable fracture or other orthopedic conditions affecting gait such as OA, fracture and arthritis (Page et al., 2007).
--Severe cognitive impairment.
- Participants with severe hemiparesis who are unable to reproduce movements accurately with the affected limb, as this may hinder active participation in the therapy(Danlami & Abdullahi, 2017; Ezendam et al., 2009).
- Individuals with physical limitations that prevent them from positioning themselves adequately to view their affected limb in the mirror during therapy sessions, as this could compromise the effectiveness of mirror therapy(Danlami & Abdullahi, 2017).
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: Constraint-Induced Movement Therapy (CIMT)
A well-defined and structured rehabilitation program that restricts the use of the unaffected limb to promote the functional recovery of the affected limb in chronic stroke patients.
|
A well-defined and structured rehabilitation program that restricts the use of the unaffected limb to promote the functional recovery of the affected limb in chronic stroke patients(Franck et al., 2019).
Sit-to-stand transitions, Indoor overground walking (forward, backward, and sideways), Weight-bearing movements in different directions: Stepping over obstacles and climbing stairs, Ideally, specific tasks to involve the paretic limb according to the activity of stroke survivors.
This task was repeated ten times as part of the therapy sessions.
Dynamic strengthening exercises like squats and lunges are integrated, progressively increasing intensity as patients gain confidence and strength.
Balance and core stability exercises, including single-leg stances and seated weight shifts on therapy balls, address postural control and stability.(Cabanas-Valdés
& Boix-Sala, 2021)
|
|
Experimental: Mirror Therapy
A specific intervention that uses a mirror to create a visual illusion of the affected limb, with the goal of improving motor function and quality of life in chronic stroke patients.
|
A specific intervention that uses a mirror to create a visual illusion of the affected limb, with the goal of improving motor function and quality of life in chronic stroke patients.
The MT protocol included 10 minutes of warm-up, 1 hour of mirror box training, and 50 minutes of functional task practice.
The warm-up activities included stretching and passive range of motion exercises.
During the mirror box training, a mirror box that reflected the image of the unaffected arm was placed in the participant's midsagittal plane.
Participants were required to symmetrically move both hands as simultaneously as possible while watching the reflection of the unaffected arm in the mirror as if it were the affected one.
To ensure that the participants focused on the reflection, the unaffected arm was placed in the mirror box, and vision of the affected arm was occluded by a vertical board placed beside the mirror box.
The activities consisted of transitive (eg, gross motor tasks, such as reaching
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional Ambulation Categories (FAC)
Time Frame: 8 weeks (baseline, fourth week and then at the end of the 8 week)
|
Functional Ambulation Categories (FAC) is a 6-point functional walking test that provides the quantitative measurement of ambulation ability, which means how much human assistance the patient needs while walking, even with personal dual assistive device
|
8 weeks (baseline, fourth week and then at the end of the 8 week)
|
|
Tinetti gait and balance score (POMA)
Time Frame: 8 weeks (baseline, fourth week and then at the end of the 8 week)
|
Tinetti Balance and Gait Assessment Performance Oriented Mobility Assessment (POMA) is a tool designed to assess the balance and gait status of a person with special reference to the potential for falling (Miodonska et al., 2018). . Scores are interpreted to reflect fall risk: Pollock et al. categories the serve self-tested mobility at low risk for participants scoring 25-28 points, moderate risk if scoring 19-24 points and high risk if scoring below 19 points on the scale. Also, patients with a score of below 26 are normally classified as high risk of falling. |
8 weeks (baseline, fourth week and then at the end of the 8 week)
|
|
Short Form Health Survey (SF-12)
Time Frame: 8 weeks (baseline, fourth week and then at the end of the 8 week)
|
The SF-12 scoring system generates two summary measures: th.e fact that the patients' disabilities are measured by the Physical Component Summary (PCS) and the Mental Component Summary (MCS).
These scores are normalized based on a mean of 50 and standard deviation of 10 to obatain meaningful numerical values.
Higher numbers represent better health related quality and those utilities with values above 50 represent superior health while below 50 represent inferior health.
(Sampogna et al., 2019).
|
8 weeks (baseline, fourth week and then at the end of the 8 week)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: IQRA Mubeen, MS IN NEUROLOGY, University of Lahore
- Study Director: Asim Rana, MS MSK, University of Lahore
Publications and helpful links
General Publications
- Campbell BCV, De Silva DA, Macleod MR, Coutts SB, Schwamm LH, Davis SM, Donnan GA. Ischaemic stroke. Nat Rev Dis Primers. 2019 Oct 10;5(1):70. doi: 10.1038/s41572-019-0118-8.
- Ezendam D, Bongers RM, Jannink MJ. Systematic review of the effectiveness of mirror therapy in upper extremity function. Disabil Rehabil. 2009;31(26):2135-49. doi: 10.3109/09638280902887768.
- Rubiera M, Aires A, Antonenko K, Lemeret S, Nolte CH, Putaala J, Schnabel RB, Tuladhar AM, Werring DJ, Zeraatkar D, Paciaroni M. European Stroke Organisation (ESO) guideline on screening for subclinical atrial fibrillation after stroke or transient ischaemic attack of undetermined origin. Eur Stroke J. 2022 Sep;7(3):VI. doi: 10.1177/23969873221099478. Epub 2022 Jun 3. Erratum In: Eur Stroke J. 2023 Mar;8(1):413. doi: 10.1177/23969873221133924.
- Iliyasu Z, Galadanci HS, Danlami KM, Salihu HM, Aliyu MH. Correlates of Postpartum Sexual Activity and Contraceptive Use in Kano, Northern Nigeria. Afr J Reprod Health. 2018 Mar;22(1):103-112. doi: 10.29063/ajrh2018/v22i1.10.
- Feigin VL, Brainin M, Norrving B, Martins S, Sacco RL, Hacke W, Fisher M, Pandian J, Lindsay P. World Stroke Organization (WSO): Global Stroke Fact Sheet 2022. Int J Stroke. 2022 Jan;17(1):18-29. doi: 10.1177/17474930211065917. Erratum In: Int J Stroke. 2022 Apr;17(4):478. doi: 10.1177/17474930221080343.
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC-UOL-/246/08/24
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
product manufactured in and exported from the U.S.
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 Stroke
-
National Assembly ClinicBayero University Kano, NigeriaRecruitingStroke | Stroke Hemorrhagic | Stroke Ischemic | Hemiparesis After StrokeNigeria
-
University of PittsburghRecruitingHemorrhagic Stroke | Embolic Stroke of Undetermined Source | Ischemic Stroke, Cryptogenic | Recurrent Ischemic Stroke | Ischemic Stroke, EmbolicUnited States
-
Mahidol UniversityNot yet recruitingIschemic Stroke | Hemorrhagic Stroke | Subacute Stroke | Chronic Stroke SurvivorsThailand
-
Mahidol UniversityRecruitingIschemic Stroke | Hemorrhagic Stroke | Subacute Stroke | Chronic Stroke PatientThailand
-
University Hospital, GhentRecruitingStroke | Stroke, Ischemic | Stroke, Acute | Stroke Sequelae | Stroke HemorrhagicBelgium
-
Moleac Pte Ltd.Not yet recruitingStroke | Stroke, Ischemic | Stroke Sequelae | Stroke, Cardiovascular | Strokes Thrombotic | Stroke, Embolic | Stroke, Cryptogenic
-
University of Illinois at ChicagoRecruitingStroke, Ischemic | Stroke Hemorrhagic | Stroke, CerebrovascularUnited States
-
IRCCS San Camillo, Venezia, ItalyRecruitingStroke | Stroke, Ischemic | Stroke Sequelae | Stroke HemorrhagicItaly
-
University Hospital HeidelbergCompletedAcute Ischemic Stroke | Acute Ischemic Stroke AIS | Acute Ischemic Stroke PatientsGermany
-
Fondazione Don Carlo Gnocchi OnlusScuola Superiore Sant'Anna di Pisa; Fondazione Policlinico Universitario Campus...Not yet recruitingStroke | Stroke Hemorrhagic | Upper Limb Rehabilitation | Stroke IschemicItaly
Clinical Trials on Constraint-Induced Movement Therapy (CIMT))
-
Cairo UniversityCompletedHand Burn | Effect of Constraint Induced Movement Therapy on Burned Dominant Hand FunctionEgypt
-
Shaare Zedek Medical CenterUnknownCerebral Palsy | HemiplegiaIsrael
-
Texas Scottish Rite Hospital for ChildrenTexas Woman's UniversityCompleted
-
Region Jönköping CountyFuturum - Academy for health and careCompletedNineteen Years of Modified CIMT in a Clinical Setting, to Improve Arm and Hand Function After StrokeStroke | Neurological Diseases or ConditionsSweden
-
Samsung Medical CenterUnknownHemiplegic Cerebral Palsy With Spasticity (Diagnosis)Korea, Republic of
-
Riphah International UniversityCompletedCerebral Palsy | Hemiplegic Cerebral PalsyPakistan
-
University Hospital of North NorwayHelse NordTerminated
-
University of LahoreNot yet recruiting
-
University of LahoreCompletedStroke | Hemiparesis | Hemiparesis After StrokePakistan
-
University of Alabama at BirminghamCompletedStroke | Rehabilitation | Recovery of Function | Lower Extremity ParesisUnited States