Under construction – not a live service
Sign in
Taking people in PakistanNo phase

Tests augmented reality and brain stimulation for balance after stroke

Tests augmented reality balance training with or without brain stimulation in chronic stroke survivors.

Plain-language title generated from the registry record
Registry title: Effects of Augmented Reality (AR) and Transcranial Direct Current Stimulation (tDCS)

Key facts

Where
Rawalpindi, PakistanSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 90 years old?

Source: NCT07629791, who can take part

Where in Pakistan

  • Railway General HospitalRawalpindi, PakistanTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Riphah International University
Trial code
NCT07629791
Record updated
20 July 2026
Original description
The aim of this randomized controlled trial is to determine the effects of Augmented Reality (AR)-based balance training on improving balance and postural control in chronic stroke survivors and whether the addition of transcranial Direct Current Stimulation (tDCS) to AR training produces superior outcomes compared to AR training alone.Read full original descriptionShow less

Effects of Augmented Reality (AR) and Transcranial Direct Current Stimulation (tDCS) on Balance and Postural Control in Chronic Stroke Survivors

The aim of this randomized controlled trial is to determine the effects of Augmented Reality (AR)-based balance training on improving balance and postural control in chronic stroke survivors and whether the addition of transcranial Direct Current Stimulation (tDCS) to AR training produces superior outcomes compared to AR training alone.

Inclusion: Balance impairment confirmed by Berg Balance Scale (BBS) score 21-44; Age between 18-90 years; Mild or no spasticity in lower limb (MAS ≤ 2); have sufficient cognition to follow the instructions provided by the therapists and the computer.

Exclusion: Other medical or psychological conditions affecting participation (e.g., severe pain, epilepsy, pacemaker); Individuals with implanted electronic devices (e.g., pacemakers), due to interaction risk with tDCS; Patients with severe cognitive deficits or visual impairments.

ClinicalTrials.gov NCT07629791