Stroke Clinical Trial
— STRIPSOfficial title:
The Effectiveness of Taping Technique Versus Conventional Techniques in Prevention of Shoulder Injuries in Patients With Acute Stroke-A Prospective, Randomized, Interventional, Outcome Blinded (PROBE Design), Parallel Design Trial
Background and Rationale: The most commonly seen disabilities in stroke patients are
shoulder injuries such as shoulder pain, glenohumeral subluxation, spasticity of shoulder
muscles, soft-tissue trauma, rotator cuff tears, and shoulder-hand syndrome.
Taping is widely used in the field of rehabilitation as both means of treatment and
prevention of sports related injuries. Scarce information is available regarding the use of
shoulder taping in preventing shoulder injuries in stroke patients. Aims:
To find out the effectiveness of taping technique with conventional treatment versus sham
taping and conventional treatment in prevention of shoulder injuries in patients with acute
stroke.
Hypothesis:
Taping technique with conventional treatment will be superior to conventional treatment
alone in preventing shoulder injuries in patients with acute stroke.
Methods Research setting: Stroke unit, department of Neurology, Christian Medical College
(CMC) Ludhiana, Punjab, India and College of Physiotherapy, CMC Ludhiana.
Study design: prospective, randomized, outcome blinded trial (PROBE design). Study period:
Prospective for 18 months from May 2009 All stroke patients with upper limb weakness within
48 hours after the ictus and with Brunnstrom's stage of recovery 1 and 2 will be included in
the study. Patients will be randomized into two groups using lottery method. The treatment
arm group(Group I) include shoulder taping with conventional techniques that is(positioning,
handling technique and passive range of motion exercises) and the control arm (Group II)
include sham taping with conventional techniques with sham taping. A total of 80 patients in
each group will be included. The plastic micropore and elastic adhesive tape will be used
for taping the affected shoulder. The sham taping will be done using the same tapes but
without stretching the concerned muscles and joints. The tapes will be changed every 3 days
and will remain for 14 days. The outcome measures are as follows; Primary: Pain: Visual
Analog Scale and Activities of daily living: Shoulder Pain and Disability Index (SPADI);
Secondary: Range of motion: using a Goniometer. The outcome will be assessed by an
independent physiotherapist who will be blinded to the clinical details. Patients will be
followed-up at 14 days and 30 days. Statistical analyses will be done using SPSS software
version 16.
Status | Completed |
Enrollment | 162 |
Est. completion date | April 2012 |
Est. primary completion date | March 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Stroke patients both ischemic and hemorrhagic with upper limb weakness within 48 hours after the ictus 2. Age over 18 years 3. Brunnstrom's stage of recovery 1 and 2 4. Patients willing to participate in the study Exclusion Criteria: 1. Patients with Glasgow coma scale of <7 2. Patients on ventilator 3. Uncooperative patients 4. Patients having previous history of shoulder injury 5. Patients with Wernicke's aphasia 6. Patients having previous history of shoulder pain 7. Any previous history of skin allergy to tape |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
India | Christian Medical College | Ludhiana | Punjab |
India | Jeyaraj D Pandian | Ludhiana | Punjab |
Lead Sponsor | Collaborator |
---|---|
Christian Medical College and Hospital, Ludhiana, India | Heart and Brain Center, Guntur, Andhra Pradesh, India, Uppal Neuro Hospital |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain: Visual Analog Scale | Visual analog scale (VAS) is an 11-point scale displayed on a 100 mm horizontal line, ranging from 0 ("No Pain") to 100 ("Worst Pain Imaginable") Shoulder pain and disability index (SPADI) is a 13-item questionnaire that consists of 2 subscales for pain (5 items) and disability (8 items), which is scored by taking an average of the 2 subscales. Scores range from 0 to 100, with higher scores indicating greater pain and disability | 14 days and 30 days | Yes |
Secondary | Passive Range of Motion (ROM) | Passive range of motion (ROM) of shoulder was measured with full circle goniometer. The normal range of movement of flexion and abduction is 180 degree. | 14 days and 30 days | No |
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