Augmented Reality for Stroke Rehabilitation

Riphah International University

Status: Completed

Conditions: Stroke/Brain Attack

Treatments: Other: Traditional Training; Other: Augmented Reality

Study type: Interventional

Funder types: Other

Identifiers

NCT06761781

REC/01997 Abrish Habib

Details and patient eligibility

About

The study aims to determine the effectiveness of Augmented reality on motor function, balance, and functional ambulation in stroke patients.

Full description

The study aims to determine the effectiveness of Augmented reality on motor function, balance, and functional ambulation in stroke patients. The emerging technology of Augmented Reality (AR), has been validated as a promising way to assist the rehabilitation training in Stroke patients. The purpose of this study is to investigate the feasibility of the AR rehabilitation system in a real-world setting. The following questions will be addressed by the present study: (a) How the Augmented reality effects motor function, balance, and functional ambulation in stroke patients? (b) how much and what types of manpower can be saved while maintaining the efficacy of training with the assistance of the AR rehabilitation? (c) how can the contact rate be reduced with the AR training? (d) how do therapists/patients experience the AR training?

Enrollment: 70 patients

Sex: All

Ages: 18 to 90 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Participants falling in this category would be recruited into the study.

1. age between 18 to 90 years who are diagnosed with ischemic brain injury, intracerebral hemorrhage shown by magnetic resonance imaging, or computed tomography after the onset of stroke;
2. with motor impairment in the upper limb, lower limb, and/or balance;
3. have no or mild spasticity on the lower limb or upper limb assessed by Modified Ashworth Scale (MAS ≤ 2); and
4. have sufficient cognition to follow the instructions provided by the therapists and the computer.

Exclusion criteria

Participants fall in this category would be excluded of the study.

1. any additional medical or psychological condition that would affect their ability to comply with the study protocol, e.g., a significant orthopedic or chronic pain condition, major post-stroke depression, epilepsy, artificial cardiac pacemaker/joint;
2. have severe shoulder/arm or hip/knee contracture/ pain and;
3. Pregnant women.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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70 participants in 2 patient groups

Augmented Reality Training

Experimental group

Description:

Augmented reality training to Experimental group

Treatment:

Other: Augmented Reality

Traditional Treatment

Active Comparator group

Description:

Task based training to the Control Group

Treatment:

Other: Traditional Training