Effect of Electrical Stimulation During Functional Proprioceptive Neuromuscular Facilitation Training on Hand Function and Spasticity Among Individuals with Sub Acute Stroke

Effect of Electrical Stimulation During Functional Proprioceptive Neuromuscular Facilitation Training on Hand Function and Spasticity Among Individuals with Sub Acute Stroke - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/12/098799

Enrollment

Registered

2025-12-10

Start date

Unknown

Completion date

Unknown

Last updated

2026-01-12

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

Conditions

Health Condition 1: I00-I99- Diseases of the circulatory system Health Condition 2: I608- Other nontraumatic subarachnoid hemorrhage Health Condition 3: I678- Other specified cerebrovascular diseases

Interventions

Intervention1: Randomised control trial: The first assessment of hand function and spasticity is conducted for all participants using the Michigan Hand Outcomes Questionnaire (MHQ) and the Chedoke Ar

Eligibility

Inclusion criteria

Inclusion criteria: 1.Trials include adults (18 years or older with clinically diagnosed stroke ) 2.Diagnosis of a first ever stroke confirmed by head CT or MRI scanning, well general condition with stabilized vital signs and normal 3.consciousness voluntary for this study with a signed informed consent 4.Both male and female patients. 5.Glasgow Coma Scale (GCS) score more than 10. 6.On Modified Modified Ashworth Scale patient scoring 1+, 2, or 3

Exclusion criteria

Exclusion criteria: 1.severe visceral organ dysfunction (e.g., heart, lung, liver, and kidney) 2.cardiac pacemaker 3.Upper limb dysfunction due to other causes 4.Recurrent stroke.

Design outcomes

Primary

Measure	Time frame
1.Improvement in hand function by Michigan Hand Outcomes Questionnaire (MHQ) and Chedoke Arm and Hand Activity Inventory-13Timepoint: 4 weeks, 5 sessions/week (total of 20 sessions)	—

Secondary

Measure	Time frame
1.Reduction of spasticity in upper extremity in sub acute stroke by modified modified ashworth scaleTimepoint: 4 weeks, 5 sessions/week (total of 20 sessions)	—

Countries

India

Contacts

Public ContactDr Ankit Jain

Amity Institute of health Allied sciences

ajain@amity.edu9999600611

Outcome results

None listed

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