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designing physiotherapy treatment for shoulder pain in stroke patients

DEVELOPING AN ULTRASOUND GUIDED THERAPEUTIC PROTOCOL IN SUBJECTS WITH POST STROKE SHOULDER PAIN

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/04/024414
Enrollment
152
Registered
2020-04-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M709- Unspecified soft tissue disorder related to use, overuse and pressure

Interventions

Intervention1: DEVELOPING AN ULTRASOUND GUIDED THERAPEUTIC INTERVENTION IN SUBJECTS WITH POST STROKE SHOULDER PAIN: LOW LEVEL LASER KINESIO TAPING EXERCISE TRAINING All subjects will undergo a 60 min

Sponsors

KIRAN PRAKASH PAPPALA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria: Unilateral ischemic or hemorrhagic stroke lesion confirmed by computerized tomography or magnetic resonance imaging , diagnosed by a Neurologist OR general physician First incidence of stroke, Pain in the affected shoulder diagnosed and referred by an orthopedician Adequate communication ability, Subjects who have motor ability to participate in exercise intervention.

Exclusion criteria

Exclusion criteria: Exclusion criteria: Shoulder pain or a history of surgery in the affected shoulder before the onset of stroke; Skin problems, wounds, or infection on the affected shoulder; A history of allergy to Kinesio Taping. Systemic neuromuscular diseases Poor cognition for cooperation during the study procedures Major cardiopulmonary or other medical diseases affecting the physical examination or daily activities. Stroke relapse /seizures during the intervention

Design outcomes

Primary

MeasureTime frame
Primary outcomes ULTRASONOGRAPHY RATING â?? to grade different pathologies of post stroke shoulder pain SPADI â?? to measure shoulder pain and disability Timepoint: USG RATING SCALE AND SPADI WILL BE MEASURED PRE TEST AND POST TEST AFTER 6 WEEKS AND AFTER 3 MONTHS FOLLOW UP

Secondary

MeasureTime frame
Secondary outcomes VAS â?? for pain DYNAMOMETER- to measure strength GONIOMETER â?? to measure ROM FMA â??UL â?? to measure upper limb motor recovery Timepoint: Pain measures will be taken every week through 6 weeks, ROM, STRENGTH measures will be taken at 3rd week and post test at 6th week. FMA-UE will be measured pre test and post test after 6 weeks. Follow up measurements will be taken after 3 months to observe the maintenance effects of this treatment protocol.

Countries

India

Contacts

Public ContactKIRAN PRAKASH PAPPALA

swatantra institute of physiotherapy and rehabilitation, Rajahmundry

kiranprakash.physio@gmail.com9949406857

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026