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

L

Louise Møldrup Nielsen

Status

Enrolling

Conditions

Stroke

Treatments

Behavioral: Usual practice
Behavioral: CO-OP intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06919315
CO-OP project

Details and patient eligibility

About

The goal of this clinical study is to examine the effectiveness of the Cognitive Orientation to daily Occupational Performance (CO-OP) in adults (45+) 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.

Enrollment

80 estimated patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • Dementia, Psychotic diagnoses, commotio, Brain tumor or degenerative neurological conditions.
  • Alkohol or drug abuse
  • Not speeking or understanding Danish

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

Experimental
Experimental group
Treatment:
Behavioral: CO-OP intervention
Control
Active Comparator group
Treatment:
Behavioral: Usual practice

Trial contacts and locations

2

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Central trial contact

Louise M Nielsen

Data sourced from clinicaltrials.gov

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