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Comparing Pain Neuroscience Education and Traditional Education on Pain, Quality of Life, and Fear of Movement in People with Chronic Shoulder Pain After Stroke

Effect of Pain Neuroscience Education Versus Conventional Patient Education on Pain, Quality of Life, Kinesiophobia and Pain Catastrophizing in Individuals with Post Stroke Chronic Shoulder Pain – A Single Blinded, Randomized Control Trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078181
Enrollment
80
Registered
2024-12-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: G892- Chronic pain, not elsewhere classified

Interventions

Intervention1: Conventional Patient Education , Pain Neuroscience Education: Intervention two groups Pain Neuroscience Education Group, Education using tailored audio-visual aids, metaphors, and bookl

Sponsors

Dr Pooja Motar Sublok
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Participants’ consent to a free participation to the study. 2. All gender 18 years old or above. 3. Chronic Stroke with duration of more than 6 months. 4. Post Stroke Chronic shoulder pain more than 3 months. 5. First ever unilateral ischaemic or haemorrhagic stroke. 6. Aadequate cognitive ability (Mini-Mental State Examination score = 24) 7. Post Stroke Chronic shoulder pain with VAS score more than 1 mm. 8. Brunnstrom recovery stages III-V

Exclusion criteria

Exclusion criteria: 1.Before Stroke Shoulder Pain, Neck Pain, Cervical Radiculopathy in the affected shoulder. 2. A history of surgery in neck or affected shoulder. 3.Acute stroke and Sub Acute Stroke. 4.Presence of language with severe comprehension deficit. 5. Participants with severe Respiratory illness, cardiopulmonary, uncontrolled hypertension or other medical diseases affecting the daily activities.29 6. Participants with impaired sensation as they will be unable to provide feedback to TENS intensity 7. Participants with Pacemaker and epilepsy contraindicated for TENS

Design outcomes

Primary

MeasureTime frame
1.The Visual Analog Scale (VAS) 2.Short-Form 36-Item Health Survey (SF-36) 3. Tampa Scale of Kinesiophobia (TSK) 4.The Pain Catastrophizing Scale (PCS) Timepoint: 0 , 6th & 8th WEEK (3 time lines)—

Secondary

MeasureTime frame
The Shoulder Pain and Disability Index (SPADI)Timepoint: 0 , 6th & 8th WEEK (3 time lines)—

Countries

India

Contacts

Public ContactDr Pooja Motar Sublok

Dept. of Orthopaedic Physiotherapy, KLE College of Physiotherapy,Hubballi

drprashantm@kledeemeduniversity.edu.in8861987516

Outcome results

None listed

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