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NCT06919315Recruiting

Effectiveness of the Cognitive Orientation to Daily Occupational Performance (CO-OP)

Effectiveness of the Cognitive Orientation to Daily Occupational Performance (CO-OP) in a Danish Rehabilitation Context

Source: ClinicalTrials.gov · Last updated 29 Jun 2026

Brief summary (registry, in English)

The goal of this clinical study is to examine the effectiveness of the Cognitive Orientation to daily Occupational Performance (CO-OP) in adults (18+) with accuired brain injury when applied in Danish rehabilitation context. The primary research question is: What is the effectiveness of the CO-OP approach on improvement of performance of daily activities (ADL) and quality of life compared to usual rehabilitation practice. Participants in the intervention group will recieve the CO-OP intervention as part of their rehabilitation in the following phases: Initial phase: Goalsetting is mandatory and based on the participant's prioritized ADL performance issues identified in their baseline COPM. Education phase: Individual education in the metacognitive Goal-Plan-Do-Check strategy. Training phase: CO-OP training that involves repetitive use of the Goal-Plan-Do-Check for problem solving and skill acquisition. The therapist employs dynamic performance analysis and guided discovery to help participants understand performance issues and formulate plans for achieving their goals. Participants then execute and evaluate these plans, with a focus on developing domain-specific cognitive strategies. The therapist actively encourages generalization and transfer of skills. Homework is mandatory. Participants in the control group will recieve usual rehabilitation practice in the following phases: Initial phase: Goalsetting is optional and may be based on previous assessment or on a conversation with the participant. Training phase: Different approaches may be taken such as observation and practice of activities or consultation about performance issues and how participants may deal with them. The therapist may guide the participant's performance verbally, physically or trough picture materials. Homework may be included.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
20 Mar 2025
Start date
2 May 2025
Primary completion date
Jul 2027
Lead sponsor
Louise Møldrup Nielsen
Diseases
Stroke
NCT number
NCT06919315

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 2 May 2025 to the primary completion date, Jul 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Alkohol or drug abuse

Other illness

  • Dementia, Psychotic diagnoses, commotio, Brain tumor or degenerative neurological conditions.

Other

  • Not speeking or understanding Danish

Who the study is looking for

  • Stroke or traumatic brain injury
  • Reffered from acute hospital or specialized rehabilitation units to municipal rehabilitation
  • Having at least on ADL performance issue

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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SiteCityCountrySite status
Rehabilitation center
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ViborgDenmarkRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.