Stroke Clinical Trial
Official title:
Analgesic Effects of Low Frequency Transcutaneous Electrical Stimulation and Therapeutic Ultrasounds on Functional Disability in Post-stroke Shoulder Pain
Brief Summary: Post-Stroke shoulder pain is a well-known complication and is responsible for the reduction in functional outcomes. A number of factors related to post-stroke shoulder pain including shoulder activity limitation, spasticity of shoulder muscles, and shoulder subluxation. Stroke patients may suffer from pain caused by the stroke itself (central post-stroke pain). Physical therapy plays an important role in the management of post-stroke shoulder pain. Different physical therapy techniques and modalities have been used in reducing pain and increasing functional outcomes in post-stroke shoulder pain patients. This study aims to provide a combined analysis of two modalities: low-frequency TENS and Therapeutic Ultrasound in terms of effects on pain and functional disability. This will be a randomized clinical trial to determine the analgesic effect of low-frequency transcutaneous electrical stimulation and therapeutic ultrasound on functional disability in post-stroke shoulder pain. The study will be conducted in accordance with ethical guidelines of Riphah International University and a convenience sampling technique will be used. Patients aged 65-84 years, with a history of pain of more than 4 weeks will be included in our study. Patients having a stroke with other neurological deficits, unstable cardiovascular diseases such as ventricular arrhythmias, and stroke patients with a history of diagnosed frozen shoulder will be excluded from the study. Subjects will be randomly allocated into three groups. Baseline assessment of pain and functional disability of patients will be done using outcome measuring tools and clinical tests. Group A will receive low-frequency TENS and therapeutic Ultrasound as a treatment, group B will receive therapeutic ultrasound and Group C will receive low-frequency TENS as a treatment. The duration of the study will be six weeks and patients will receive a total of 12 treatment sessions (3 sessions per week for 4 weeks and then follow-up will be done for the next 2 weeks) and the duration of each session will be of 20-25 minutes. After 12 sessions, a final assessment will be done and the results will be analyzed. Frequencies and mean standard deviation will be measured, and parametric and non-parametric tests will be applied.
Status | Recruiting |
Enrollment | 48 |
Est. completion date | October 1, 2023 |
Est. primary completion date | August 15, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 65 Years to 84 Years |
Eligibility | Inclusion Criteria: - Age 65-84 years(23) - Both genders male and female will be included - Ischemic and hemorrhagic both types of strokes will be included - Patients with a history of shoulder pain Exclusion Criteria: - Patients with another neurological disease - Patients with unstable cardiovascular disease such as ventricular arrhythmias - Patients with a history of traumatic brain injury Patients with a history of traumatic brain injury - Any contraindications for UST or TENS therapy |
Country | Name | City | State |
---|---|---|---|
Pakistan | Bahawal Victoria Hospital | Bahawalpur | Punjab |
Lead Sponsor | Collaborator |
---|---|
Riphah International University |
Pakistan,
Broeks JG, Lankhorst GJ, Rumping K, Prevo AJ. The long-term outcome of arm function after stroke: results of a follow-up study. Disabil Rehabil. 1999 Aug;21(8):357-64. doi: 10.1080/096382899297459. — View Citation
Celik EC, Erhan B, Gunduz B, Lakse E. The effect of low-frequency TENS in the treatment of neuropathic pain in patients with spinal cord injury. Spinal Cord. 2013 Apr;51(4):334-7. doi: 10.1038/sc.2012.159. Epub 2013 Jan 8. — View Citation
Dyer S, Mordaunt DA, Adey-Wakeling Z. Interventions for Post-Stroke Shoulder Pain: An Overview of Systematic Reviews. Int J Gen Med. 2020 Dec 7;13:1411-1426. doi: 10.2147/IJGM.S200929. eCollection 2020. — View Citation
Ekim A, Armagan O, Oner C. [Efficiency of TENS treatment in hemiplegic shoulder pain: a placebo controlled study]. Agri. 2008 Jan;20(1):41-6. Turkish. — View Citation
Eslamian F, Farhoudi M, Jahanjoo F, Sadeghi-Hokmabadi E, Darabi P. Electrical interferential current stimulation versus electrical acupuncture in management of hemiplegic shoulder pain and disability following ischemic stroke-a randomized clinical trial. Arch Physiother. 2020 Jan 10;10:2. doi: 10.1186/s40945-019-0071-6. eCollection 2020. — View Citation
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Lindgren I, Jonsson AC, Norrving B, Lindgren A. Shoulder pain after stroke: a prospective population-based study. Stroke. 2007 Feb;38(2):343-8. doi: 10.1161/01.STR.0000254598.16739.4e. Epub 2006 Dec 21. — View Citation
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* Note: There are 11 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | .Numerical Pain Rating Scale | We used an 11-point numerical pain rating scale. (Where 0 = no pain; 10 = maximum pain) to assess the intensity of spontaneous HSP. The patients were required not to take analgesics or muscle relaxants for 24 h prior to the assessment | 6 weeks | |
Primary | Shoulder Pain and Disability Index | shoulder pain and disability index is a 13 items subjective questionnaire. Which is used to measure the level of pain and disability associated with shoulder pathologies. It has two subsets: Pain (5 items) and disability (8 items) to assess functional status of individuals with shoulder problems | 6 weeks | |
Primary | Disabilities of Arm, Shoulder Hand questionnaire | The Disabilities of the Arm, Shoulder and Hand (DASH) Outcome Measure is a 30-item, self- report questionnaire designed to measure physical function and symptoms in patients with any or several musculoskeletal disorders of the upper limb. The questionnaire was designed to help describe the disability experienced by people with upper-limb disorders and also to monitor changes in symptoms and function over time | 6 weeks |
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