Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06058351

ABI-aftercare in Motion: Multidisciplinary Aftercare in the Home Environment in Patients With Acquired Brain Injury

Led by Majanka H. Heijenbrok-Kal, PhD · Updated on 2025-08-29

60

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

M

Majanka H. Heijenbrok-Kal, PhD

Lead Sponsor

N

Netherlands Brain Foundation

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this implementation study is to improve aftercare for patients with ABI receiving outpatient rehabilitation. The ABI-motion program was developed to improve and active lifestyle and to prevent persistent complaints after ABI and poor HR-QoL.The main questions it aims to answer are: * Is the ABI-motion program feasible? * What are the health benefits of the ABI-motion program? Participants will receive brain education, a joint therapy session with a physical or occupational or movement therapist and a buddy from a patient support organization during outpatient rehabilitation, followed by community buddy support after discharge from outpatient rehabilitation, and follow-up by a rehabilitation physician.

CONDITIONS

Official Title

ABI-aftercare in Motion: Multidisciplinary Aftercare in the Home Environment in Patients With Acquired Brain Injury

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with ABI
  • Currently following an outpatient rehabilitation program for ABI in Rijndam Rehabilitation
Not Eligible

You will not qualify if you...

  • Having a contra-indication for participation in moderate to vigorous exercise
  • Life expectancy less than 1 year
  • Incapacitated persons

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Rijndam Rehabilitation

Rotterdam, Netherlands, 3015LJ

Actively Recruiting

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Research Team

M

Majanka H Heijenbrok-Kal, PhD

CONTACT

E

Erik Grauwmeijer, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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