Indonesian Version of Oxford Cognitive Screen-Plus Test in Stroke Patient

NCT07817784 | Not Yet Recruiting DMC

• 1 other identifier: IKFR-202604.02
• Study Type: observational
• Target: 75
• Locations: 0 countries
• Sites: N/A

Brief Summary

The incidence of stroke increases every year throughout the world. Neuropsychological assessment is the best way to identify post-stroke cognitive dysfunction. The importance of cognitive function in the post stroke rehabilitation program process requires a tool that can detect cognitive disorders more specifically and more sensitively. The investigator aim in this study was to develop Indonesian version of the OCS - Plus among stroke patient in Indonesia.

Conditions

Post Stroke; Cognitive Assessment

Keywords

Cognitive Assessment; Post Stroke; Rehabilitation

Outcome Measures

Primary Outcomes (1)

• Validity and Reliability of Indonesian OCS Plus

  Task-specific OCS-Plus convergent and divergent validity was examined against task-matched validated MoCA tests in a pre-registered Spearman's Rho correlation analyses. Investigator's aimed for correlations \>0.30 to demarcate convergence. The reliability coefficient calculation technique used here is to use the Alpha Reliability Coefficient.

  T0 - Baseline assessment (Day 1) -. Informed consent and Demographic -. MoCA-Ina -. Indonesian OCS-Plus T1 - Retest (48 hours after T0) -.Indonesian OCS-Plus repeated under standardized conditions -.No cognitive rehabilitation intervention between T0-T1

Study Arms (1)

Validity/Reliability Group

This group contain post stroke patient that will be given task to work on OCS Plus in accordance with the procedure from the aplication

Device: OCS Plus Assessment

Interventions

OCS Plus Assessment DEVICE

Subject is going to carry out Indonesian OCS Plus assessment in accordance with the procedure given by the application.

Validity/Reliability Group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

The target population consists of stroke patients in West Java. The accessible population includes stroke patients undergoing treatment at the medical rehabilitation clinic and neurology clinic at RSUP Dr. Hasan Sadikin Bandung

You may qualify if:

• Male or female18 years of age or older
• Subacute and chronic stroke patients
• Able to understand instructions
• Able to read
• Can speak Indonesian well
• Willing to take part in research

You may not qualify if:

• Have uncorrected severe visual and hearing impairments
• Have cognitive rehabilitation before research
• Inability to maintain concentration for approximately 30 minutes

Sponsors & Collaborators

• Universitas Padjadjaran: lead
• University of Oxford: collaborator

MeSH Terms

Interventions

Physical Examination

Intervention Hierarchy (Ancestors)

Diagnostic Techniques and Procedures; Diagnosis

Study Officials

• Vitriana Biben, Doctoral

  Universitas Padjadjaran

  STUDY DIRECTOR

Central Study Contacts

Muhammad Luthfi Dharmawan, Subspecialist Degree

CONTACT

+6281122220052; m.luthfi@unpad.ac.id

Nofri Yandri, Medical Doctor

CONTACT

+6281267271717; nofriy14@gmail.com

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 20, 2026
• First Posted: September 14, 2026
• Study Start: September 1, 2026
• Primary Completion: October 1, 2026
• Study Completion (Estimated): December 31, 2026
• Last Updated: September 14, 2026

Record last verified: 2026-08