Implementation of a home-based computerized cognitive rehabilitation program for patients with acquired brain injury

Implementation of a home-based computerized cognitive rehabilitation program for patients with acquired brain injury - CoRe@Home

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON57345

Enrollment

Registered

2025-03-20

Start date

2025-05-28

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acquired brain injury

Interventions

The intervention consists of a combination of strategy training and the evidence-based CCR ReHaCom-Online. The CCR program consists of a selection of 29 modules with various levels, making the thera

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - receiving outpatient rehabilitation for acquired brain injury (ABI) - age at least 18 years - no cognitive complaints before ABI - patient has sufficient knowledge of the Dutch or English language - internet access

Exclusion criteria

Exclusion criteria: -incapacitated or progressive neurological disease, such as Alzheimer's disease

Design outcomes

Primary

Measure	Time frame
Primary outcome measures are sustained and divided attention and working memory, which will be measured with objective neuropsychological tests. For general cognitive screening, the Montreal Cognitive Assessment (MoCA) will be used. Changes in visual selective attention, processing speed and concentration are measured with the D2 test. Changes in visual attention, executive function (divided attention) and processing speed are measured with the TMT A & B. The Stroop Test measures mental speed, executive attention and response inhibition. Attention and working memory are examined using the digit span forward (DSF) and digit span backward (DSB). Together with 'Arithmetics', an index for working memory can be calculated.	—

Measure

Time frame

Primary outcome measures are sustained and divided attention and working memory, which will be measured with objective neuropsychological tests. For general cognitive screening, the Montreal Cognitive Assessment (MoCA) will be used. Changes in visual selective attention, processing speed and concentration are measured with the D2 test. Changes in visual attention, executive function (divided attention) and processing speed are measured with the TMT A & B. The Stroop Test measures mental speed, executive attention and response inhibition. Attention and working memory are examined using the digit span forward (DSF) and digit span backward (DSB). Together with 'Arithmetics', an index for working memory can be calculated.

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Secondary

Measure	Time frame
Secondary outcome measures are self-management, subjective cognitive complaints, mood, fatigue and quality of life, which will be measured with standardized questionnaires. The feasibility of the blended care pathway will be qualitatively evaluated by documenting compliance with the protocol (number of completed sessions, dropouts), the outcomes of focus groups (barriers and facilitators), an evaluation form (yet to be developed) and a standardized questionnaire, with which the appreciation of the process of implementation by therapists is evaluated.	—

Measure

Time frame

Secondary outcome measures are self-management, subjective cognitive complaints, mood, fatigue and quality of life, which will be measured with standardized questionnaires. The feasibility of the blended care pathway will be qualitatively evaluated by documenting compliance with the protocol (number of completed sessions, dropouts), the outcomes of focus groups (barriers and facilitators), an evaluation form (yet to be developed) and a standardized questionnaire, with which the appreciation of the process of implementation by therapists is evaluated.

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Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jul 3, 2026