StrokeNCT05931185
Effects of Low Frequency TENS and Therapeutic Ultrasound in Post-stroke Shoulder Pain
A study testing low frequency transcutaneous electrical stimulation and Therapeutic Ultrasound, Therapeutic Ultrasound and Low frequency transcutaneous electrical stimulation in people with Stroke and Shoulder Pain, run by Riphah International University at 1 site in Pakistan.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 65 to 84 years
- Conditions the study is for
- Stroke, Shoulder Pain
- What is being tested?
- low frequency transcutaneous electrical stimulation and Therapeutic Ultrasound, Therapeutic Ultrasound and Low frequency transcutaneous electrical stimulation
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 48 participants
- Where
- 1 sitePakistan
- Study dates
- 11 Nov 2022to 1 Oct 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 65 to 84 years
- All sexes
- No healthy volunteers
- Older adult
Who may be able to join
- 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
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country.
Pakistan1 site, 1 recruiting
- Recruiting
Bahawal Victoria Hospital
Bahawalpur, Punjab Province, 63100
muhammad irshad, 03336352593
toqeer zulfiqar, DPT
About this study
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.
Read the detailed description
Cerebral vascular accidents (CVAs) are the second most common cause of death in developed nations, according to the World Health Organization.It is a significant factor in disability because it causes paralysis and cognitive impairments in the population that survives. According to data from the literature, 25% of stroke patients pass away within a few weeks.Shoulder pain is exasperating complication after stroke and responsible for the longer stay in the rehabilitation department. The incidence varies from 9%-40.Post-Stroke shoulder pain decreased functional outcome, and quality of life.Post-stroke muscle weakness and spasticity lead to shoulder instability and immobility. The etiology of shoulder pain after stroke is multifactorial complex regional pain syndrome, shoulder joint subluxation, adhesive capsulitis, spasticity, and shoulder muscles weakness.Etiological intricacy makes it necessary to use a stroke-specific approach rather than always expanding the musculoskeletal knowledge base.
Presence of hemiplegic shoulder pain is strongly associated poor recovery of arm function in the first 12 weeks after stroke.It may be a sign of brachial plexus damage if there are aberrant motor recovery patterns, spasticity or particularly severe localized atrophy. A pre-existing ailment like osteoarthritis may worsen as a result of improper management of a hemiplegic limb. Therefore, hemiplegic shoulder pain may be caused by pre-morbid shoulder illness.Physical therapy has been shown to be very effective in treating post-stroke shoulder pain. A variety of techniques and treatment modalities are use around the world to alleviate the post-stroke shoulder pain. Of particular interest to this research are two electrotherapy modalities low frequency transcutaneous electrical stimulation and Therapeutic Ultrasound will be treatment option.
TENS therapy together with conventional rehabilitation could be used as a good alternative therapy in patients with hemiplegic shoulder pain.There is wide spread use of TENS throughout health care and it is a common treatment modality for musculoskeletal pain. The TENS settings are based on the gate control theory of pain. TENS is agree to produce a significant reduction in pain. Transcutaneous electrical nerve stimulation (TENS) is an inexpensive, noninvasive, self-administered technique that is use as an adjunct to medication. TENS treatment is rarely associated with negative side effects and has been reported to be effective in patients with neuropathic pain. Most studies evaluated the effect of high-frequency or low-frequency TENS (LF-TENS).The study aim is to investigate the effect of LF-TENS on the treatment of neuropathic pain in patients with post-stroke shoulder pain.
Therapeutic Ultrasound a physical therapy agent commonly used to increase temperature in deep tissue. The biologic effects observed when mammalian tissues are expose to ultrasound include changes in blood flow rates, tissue metabolism, the extensibility of connective tissue, and tissue regeneration. Thermal effects of therapeutic ultrasound reduces pain, swelling and improve ROM. When treating knee, shoulder, and hip pain, therapeutic ultrasound is routinely utilize in conjunction with other physiotherapeutic methods. The body of research on knee arthritis is very strong, and there is some evidence that therapeutic ultrasound is effective although there is debate about whether ultrasound should be delivered continuously or in pulses. Although ultrasound therapy alone may not have much of an effect on functional improvement, it can be a fair adjunct to take into account when combined with other widely used modalities.
The current study aims to evaluate and generalize the comparative effects of low frequency transcutaneous electrical stimulation combined with therapeutic ultrasound and therapeutic ultrasound and low frequency TENS alone in our settings. It is suggested that low frequency TENS with therapeutic ultrasound would provide a clinically and statistically significant benefit over a therapeutic ultrasound and low frequency TENS alone for patients with functional disability in post stroke shoulder pain. The purpose of the study is to determine an appropriate and cost-effective rehabilitation protocol for patients with functional disability in post-stroke shoulder pain.
Literature review.
A randomize clinical trial conducted in 2010 to evaluate the effect of therapeutic modalities on patients with post stroke shoulder pain. 45 patients were selected randomly with post stroke shoulder pain. Patients were randomly assigned into group A and group B .Group A patients treated by TENS, NASIAD, Exercise and ADLs instructions and group B received therapeutic ultrasound, NSAID, Exercise and ADLs instructions for 5 visits after every two weeks interval. The study recommended that TENS is more effective than therapeutic ultrasound.
A single blind, randomized controlled trial was conducted in 2017 determine the effect of EMG-triggered neuromuscular electrical stimulation with bilateral arm training on hemiplegic shoulder pain and arm function after stroke. Thirty-eight patients with post-stroke shoulder pain were randomized to EMG-triggered NMES or TENS. Both groups received electrical stimulation followed by bilateral arm training 3 times a week for 4 weeks. Primary outcome measures included a vertical numerical rating scale supplemented by a face rating scale and the short form of the Brief Pain Inventory. Secondary outcome measures were the upper extremity subscale of the Fugl-Meyer rating and pain-free passive shoulder range of motion. All outcomes were measured before treatment, post treatment. Two-way mixed repeated- measures ANOVAs were used to examine treatment effects. EMG-triggered NMES with bilateral arm training showed greater immediate and sustained effects than TENS with bilateral arm training on shoulder pain and damage in chronic and subacute stroke patients with hemiplegic shoulder pain.
A research was conducted to evaluate the effectiveness of high-intensity laser therapy in the treatment of post-stroke patients with hemiplegic shoulder pain. A study was designed as a prospective, randomize clinical trial. Forty-four patients with hemiplegic shoulder pain accompanied by partial thickness rotator cuff tear were randomly divided into high intensity lesser therapy and control groups. High intensity lesser therapy group and control group treated with multidisciplinary rehabilitation and therapeutic exercise program in addition to this three session of intervention per week for three weeks received by high intensity lesser therapy group. High intensity lesser therapy treatment significantly decrease pain ,increase range of motion and functional independence as compare to control group.
- Conditions
- Stroke, Shoulder Pain
- Being tested
- low frequency transcutaneous electrical stimulation and Therapeutic Ultrasound, Therapeutic Ultrasound, Low frequency transcutaneous electrical stimulation
- Keywords
- Post-Stroke shoulder pain, Low frequency TENS, Therapeutic ultrasound, Functional disability
- Medical subject headings
- Stroke, Shoulder Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
low frequency transcutaneous electrical stimulation and Therapeutic UltrasoundOther
patients will receive low-frequency transcutaneous electrical stimulation for 15 minutes and therapeutic Ultrasound for 10 minutes as a treatment 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 total duration of each session will be of 25 minutes.
Therapeutic UltrasoundOther
patients will receive a therapeutic ultrasound for 10 minutes three times a week for 4 weeks and then follow-up will be done for the next 2 weeks
Low frequency transcutaneous electrical stimulationOther
participants will receive low-frequency transcutaneous electrical stimulation for 15 minutes three times a week for 4 weeks and then follow-up will be done for the next 2 weeks
| Study group | Role | What they receive |
|---|---|---|
| Low frequency transcutaneous electrical stimulation and Therapeutic Ultrasound | Experimental | participant will receive low frequency transcutaneous electrical stimulation and therapeutic Ultrasound as a treatment Receives: Other: low frequency transcutaneous electrical stimulation and Therapeutic Ultrasound |
| Therapeutic Ultrasound | Active comparator | patients will receive therapeutic ultrasound as a treatment Receives: Other: Therapeutic Ultrasound |
| Low frequency transcutaneous electrical stimulation | Active comparator | participant will receive low frequency transcutaneous electrical stimulation Receives: Other: Low frequency transcutaneous electrical stimulation |
What is being measured
The primary outcome is the main question the study is designed to answer.
.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
Measured: 6 weeks
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
Measured: 6 weeks
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
Measured: 6 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Jul 2023
- Study start11 Nov 2022
- Primary completion15 Aug 2023 (estimated)
- Study completion1 Oct 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (11)Papers the sponsor has linked to this study.
- Other trials for StrokeStudies of the same condition, open and under way.
- More trials run by Riphah International UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 48 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Riphah International University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- hira jabeen, Principal investigator, Riphah International University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05931185
- Sponsor's protocol ID
- REC/RCR & AHS/23/0201
- Status last verified
- Jul 2023
- First submitted
- 26 Jun 2023
- Last updated
- 14 Jul 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
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.
PubMed 10503976Lindgren 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.
PubMed 17185637Eslamian 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.
PubMed 31938571Dyer 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.
PubMed 33324087Walsh K. Management of shoulder pain in patients with stroke. Postgrad Med J. 2001 Oct;77(912):645-9. doi: 10.1136/pmj.77.912.645.
PubMed 11571371Griffin JW. Hemiplegic shoulder pain. Phys Ther. 1986 Dec;66(12):1884-93. doi: 10.1093/ptj/66.12.1884.
PubMed 2431421Ekim 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.
PubMed 18338278Vecchio P, Cave M, King V, Adebajo AO, Smith M, Hazleman BL. A double-blind study of the effectiveness of low level laser treatment of rotator cuff tendinitis. Br J Rheumatol. 1993 Aug;32(8):740-2. doi: 10.1093/rheumatology/32.8.740.
PubMed 8348278Vlak T, Jakelic K, Jajic I. [Comparative study of the effectiveness of lasers and cryotherapy in the treatment of painful shoulder syndrome]. Reumatizam. 1994;41(1):9-15. Croatian.
PubMed 7638444Celik 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.
PubMed 23295472van der Windt DAWM, van der Heijden GJMG, van den Berg SGM, Ter Riet G, de Winter AF, Bouter LM. Ultrasound therapy for musculoskeletal disorders: a systematic review. Pain. 1999 Jun;81(3):257-271. doi: 10.1016/S0304-3959(99)00016-0.
PubMed 10431713
Study at a glance
From the registry record, last updated by the sponsor on 14 Jul 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Analgesic Effects of Low Frequency Transcutaneous Electrical Stimulation and Therapeutic Ultrasounds on Functional Disability in Post-stroke Shoulder Pain
- ClinicalTrials.gov ID
- NCT05931185
- Acronym / sponsor ID
- REC/RCR & AHS/23/0201
- Conditions
- Stroke, Shoulder Pain
- Keywords
- Post-Stroke shoulder pain, Low frequency TENS, Therapeutic ultrasound, Functional disability
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 48 participants (estimated)
- Lead sponsor
- Riphah International UniversityUniversity, hospital or other
- Study start
- 11 Nov 2022 (actual)
- Primary completion
- 15 Aug 2023 (estimated)
- Study completion
- 1 Oct 2023 (estimated)
- First posted
- 5 Jul 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
Cerebral vascular accidents (CVAs) are the second most common cause of death in developed nations, according to the World Health Organization.It is a significant factor in disability because it causes paralysis and cognitive impairments in the population that survives. According to data from the literature, 25% of stroke patients pass away within a few weeks.Shoulder pain is exasperating complication after stroke and responsible for the longer stay in the rehabilitation department. The incidence varies from 9%-40.Post-Stroke shoulder pain decreased functional outcome, and quality of life.Post-stroke muscle weakness and spasticity lead to shoulder instability and immobility. The etiology of shoulder pain after stroke is multifactorial complex regional pain syndrome, shoulder joint subluxation, adhesive capsulitis, spasticity, and shoulder muscles weakness.Etiological intricacy makes it necessary to use a stroke-specific approach rather than always expanding the musculoskeletal knowledge base.
Presence of hemiplegic shoulder pain is strongly associated poor recovery of arm function in the first 12 weeks after stroke.It may be a sign of brachial plexus damage if there are aberrant motor recovery patterns, spasticity or particularly severe localized atrophy. A pre-existing ailment like osteoarthritis may worsen as a result of improper management of a hemiplegic limb. Therefore, hemiplegic shoulder pain may be caused by pre-morbid shoulder illness.Physical therapy has been shown to be very effective in treating post-stroke shoulder pain. A variety of techniques and treatment modalities are use around the world to alleviate the post-stroke shoulder pain. Of particular interest to this research are two electrotherapy modalities low frequency transcutaneous electrical stimulation and Therapeutic Ultrasound will be treatment option.
TENS therapy together with conventional rehabilitation could be used as a good alternative therapy in patients with hemiplegic shoulder pain.There is wide spread use of TENS throughout health care and it is a common treatment modality for musculoskeletal pain. The TENS settings are based on the gate control theory of pain. TENS is agree to produce a significant reduction in pain. Transcutaneous electrical nerve stimulation (TENS) is an inexpensive, noninvasive, self-administered technique that is use as an adjunct to medication. TENS treatment is rarely associated with negative side effects and has been reported to be effective in patients with neuropathic pain. Most studies evaluated the effect of high-frequency or low-frequency TENS (LF-TENS).The study aim is to investigate the effect of LF-TENS on the treatment of neuropathic pain in patients with post-stroke shoulder pain.
Therapeutic Ultrasound a physical therapy agent commonly used to increase temperature in deep tissue. The biologic effects observed when mammalian tissues are expose to ultrasound include changes in blood flow rates, tissue metabolism, the extensibility of connective tissue, and tissue regeneration. Thermal effects of therapeutic ultrasound reduces pain, swelling and improve ROM. When treating knee, shoulder, and hip pain, therapeutic ultrasound is routinely utilize in conjunction with other physiotherapeutic methods. The body of research on knee arthritis is very strong, and there is some evidence that therapeutic ultrasound is effective although there is debate about whether ultrasound should be delivered continuously or in pulses. Although ultrasound therapy alone may not have much of an effect on functional improvement, it can be a fair adjunct to take into account when combined with other widely used modalities.
The current study aims to evaluate and generalize the comparative effects of low frequency transcutaneous electrical stimulation combined with therapeutic ultrasound and therapeutic ultrasound and low frequency TENS alone in our settings. It is suggested that low frequency TENS with therapeutic ultrasound would provide a clinically and statistically significant benefit over a therapeutic ultrasound and low frequency TENS alone for patients with functional disability in post stroke shoulder pain. The purpose of the study is to determine an appropriate and cost-effective rehabilitation protocol for patients with functional disability in post-stroke shoulder pain.
Literature review.
A randomize clinical trial conducted in 2010 to evaluate the effect of therapeutic modalities on patients with post stroke shoulder pain. 45 patients were selected randomly with post stroke shoulder pain. Patients were randomly assigned into group A and group B .Group A patients treated by TENS, NASIAD, Exercise and ADLs instructions and group B received therapeutic ultrasound, NSAID, Exercise and ADLs instructions for 5 visits after every two weeks interval. The study recommended that TENS is more effective than therapeutic ultrasound.
A single blind, randomized controlled trial was conducted in 2017 determine the effect of EMG-triggered neuromuscular electrical stimulation with bilateral arm training on hemiplegic shoulder pain and arm function after stroke. Thirty-eight patients with post-stroke shoulder pain were randomized to EMG-triggered NMES or TENS. Both groups received electrical stimulation followed by bilateral arm training 3 times a week for 4 weeks. Primary outcome measures included a vertical numerical rating scale supplemented by a face rating scale and the short form of the Brief Pain Inventory. Secondary outcome measures were the upper extremity subscale of the Fugl-Meyer rating and pain-free passive shoulder range of motion. All outcomes were measured before treatment, post treatment. Two-way mixed repeated- measures ANOVAs were used to examine treatment effects. EMG-triggered NMES with bilateral arm training showed greater immediate and sustained effects than TENS with bilateral arm training on shoulder pain and damage in chronic and subacute stroke patients with hemiplegic shoulder pain.
A research was conducted to evaluate the effectiveness of high-intensity laser therapy in the treatment of post-stroke patients with hemiplegic shoulder pain. A study was designed as a prospective, randomize clinical trial. Forty-four patients with hemiplegic shoulder pain accompanied by partial thickness rotator cuff tear were randomly divided into high intensity lesser therapy and control groups. High intensity lesser therapy group and control group treated with multidisciplinary rehabilitation and therapeutic exercise program in addition to this three session of intervention per week for three weeks received by high intensity lesser therapy group. High intensity lesser therapy treatment significantly decrease pain ,increase range of motion and functional independence as compare to control group.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Low frequency transcutaneous electrical stimulation and Therapeutic Ultrasound | Experimental | Other: low frequency transcutaneous electrical stimulation and Therapeutic Ultrasoundparticipant will receive low frequency transcutaneous electrical stimulation and therapeutic Ultrasound as a treatment |
| Therapeutic Ultrasound | Active comparator | Other: Therapeutic Ultrasoundpatients will receive therapeutic ultrasound as a treatment |
| Low frequency transcutaneous electrical stimulation | Active comparator | Other: Low frequency transcutaneous electrical stimulationparticipant will receive low frequency transcutaneous electrical stimulation |
Who may qualify
- Ages
- 65 to 84 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Older adult
Key inclusion criteria (4 listed)
- Age 65-84 years(23)
Key exclusion criteria (4 listed)
- Patients with another neurological disease
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| low frequency transcutaneous electrical stimulation and Therapeutic Ultrasoundpatients will receive low-frequency transcutaneous electrical stimulation for 15 minutes and therapeutic Ultrasound for 10 minutes as a treatment 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 total duration of each session will be of 25 minutes. | Other | Low frequency transcutaneous electrical stimulation and Therapeutic Ultrasound |
| Therapeutic Ultrasoundpatients will receive a therapeutic ultrasound for 10 minutes three times a week for 4 weeks and then follow-up will be done for the next 2 weeks | Other | Therapeutic Ultrasound |
| Low frequency transcutaneous electrical stimulationparticipants will receive low-frequency transcutaneous electrical stimulation for 15 minutes three times a week for 4 weeks and then follow-up will be done for the next 2 weeks | Other | Low frequency transcutaneous electrical stimulation |
Primary outcome
.Numerical Pain Rating Scale
Time frame: 6 weeks
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
Shoulder Pain and Disability Index
Time frame: 6 weeks
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
Disabilities of Arm, Shoulder Hand questionnaire
Time frame: 6 weeks
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
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Jul 2023.
- Background: PubMed 10503976Broeks 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.
- Background: PubMed 17185637Lindgren 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.
- Background: PubMed 31938571Eslamian 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.
- Background: PubMed 33324087Dyer 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.
- Background: PubMed 11571371Walsh K. Management of shoulder pain in patients with stroke. Postgrad Med J. 2001 Oct;77(912):645-9. doi: 10.1136/pmj.77.912.645.
- Background: PubMed 2431421Griffin JW. Hemiplegic shoulder pain. Phys Ther. 1986 Dec;66(12):1884-93. doi: 10.1093/ptj/66.12.1884.
- Background: PubMed 18338278Ekim 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.
- Background: PubMed 8348278Vecchio P, Cave M, King V, Adebajo AO, Smith M, Hazleman BL. A double-blind study of the effectiveness of low level laser treatment of rotator cuff tendinitis. Br J Rheumatol. 1993 Aug;32(8):740-2. doi: 10.1093/rheumatology/32.8.740.
- Background: PubMed 7638444Vlak T, Jakelic K, Jajic I. [Comparative study of the effectiveness of lasers and cryotherapy in the treatment of painful shoulder syndrome]. Reumatizam. 1994;41(1):9-15. Croatian.
- Background: PubMed 23295472Celik 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.
- Background: PubMed 10431713van der Windt DAWM, van der Heijden GJMG, van den Berg SGM, Ter Riet G, de Winter AF, Bouter LM. Ultrasound therapy for musculoskeletal disorders: a systematic review. Pain. 1999 Jun;81(3):257-271. doi: 10.1016/S0304-3959(99)00016-0.
- Individual participant dataSharing planned: No
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Acute Ischemic Stroke, Basilar Artery Occlusion
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
hira jabeen principal investigator
Riphah International University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing low frequency transcutaneous electrical stimulation and Therapeutic Ultrasound, Therapeutic Ultrasound and Low frequency transcutaneous electrical stimulation in people with Stroke and Shoulder Pain, run by Riphah International University at 1 site in Pakistan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 14 Jul 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact hira jabeen (03234116506, hira.jabeen@riphah.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
.Numerical Pain Rating Scale (time frame: 6 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05931185, which also lists 11 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jul 2023.