Tele-Rehabilitation vs Conventional Rehabilitation for Cognitive Improvement in Stroke Survivors.

Sponsor
Riphah International University
Study ID
NCT07504276
Status
Recruiting

Conditions

  • Cognitive Impairment
  • Post-Stroke Cognitive Impairment
  • Stroke

Eligibility Criteria

Sex
ALL
Age
50 Years - 80 Years
Healthy Volunteers
Not accepted

Interventions

  • Tele-rehabilitation — BEHAVIORAL
    Cognitive rehabilitation exercises delivered remotely using video-based sessions, targeting attention, memory, executive function, and processing speed. Sessions will be conducted over 8 weeks.
  • Conventional Rehabilitation — BEHAVIORAL
    In-person cognitive rehabilitation exercises targeting attention, memory, executive function, and processing speed delivered in a clinical setting for 8 weeks.

Study Details

This study aims to: * Compare tele-rehabilitation and conventional rehabilitation for cognitive improvement after stroke. * Evaluate changes in cognitive function using standardized assessment tools. * Determine whether tele-rehabilitation is as effective as conventional therapy. * Improve evidence-based rehabilitation strategies for stroke survivors.

Key Dates

First listed
Mar 31, 2026
Start date
Mar 31, 2026
Status verified
Apr 2026
Primary completion
Jul 30, 2026
Completion
Aug 15, 2026

Study Design

Enrollment
32 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Tele-Rehabilitation Group
    Participants will receive structured cognitive rehabilitation remotely through telecommunication platforms for 8 weeks. Sessions will be conducted with comparable frequency and intensity to the control group.
  • Active Comparator: Conventional Rehabilitation Group
    Participants will receive face-to-face cognitive rehabilitation sessions in a clinical setting for 8 weeks with similar frequency and duration as the tele-rehabilitation group.

Primary Outcome Measure

Change in Cognitive Function Measured by Montreal Cognitive Assessment (MoCA) [ Time Frame: Baseline ]

Central Contacts

Find similar trials

Related Studies