PoRI Clinical Trial

Conditions

• Post Stroke
• Post Stroke Hand Rehabilitation

Eligibility Criteria

Sex

ALL

Age

18 Years - N/A

Healthy Volunteers

Not accepted

Interventions

• Portable Rehabilitation Interface (PoRI) — DEVICE
  Handheld device known as the Portable Rehabilitation Interface (PoRI) that moves the hand of patients with sensorimotor hand dysfunction

Study Details

This randomized clinical trial compares the Portable Rehabilitation Interface (PoRI) device for rehabilitation of hand motor function in post-stroke patients with conventional hand therapy.

Key Dates

Start date

Mar 23, 2026

Status verified

Mar 2026

Primary completion

Sep 30, 2027

Completion

Sep 30, 2027

Study Design

Enrollment

12 participants (estimated)

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Arms

• Experimental: Portable Rehabilitation Interface (PoRI) + Conventional Therapy
  Participants will receive seven 20-minute sessions with the PoRI device within 10 days during the course of care in addition to conventional therapy (standard of care) for 1 hour per day, 5 days per week for 2 to 3 weeks.
• No Intervention: Conventional Therapy
  Participants will receive 1 hour sessions, 5 days per week for 2 to 3 weeks using conventional therapy (standard of care)

Primary Outcome Measure

Fugl-Meyer Assessment (FMA) score [ Time Frame: Baseline and Week 2-3 ]

Central Contacts

• Necolle Morgado-Vega
  203-843-5733
  [email protected]
• Gregory Roytman
  815-382-0687
  [email protected]

Locations (1)

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