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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMajanka H. Heijenbrok-Kal, PhD

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosed with ABI

Follows an outpatient rehabilitation program for ABI in Rijndam Rehabilitation

Disqualifiers

Having a contra-indication for participation in moderate to vigorous exercise

Life expectancy < 1 year

Incapacitated persons

Trial design

Design model

Sequential

Treatments tested in this trial

  • ABI-motion program

    Behavioral

    The ABI-motion program strengthens the cooperation between outpatient rehabilitation professionals and community care providers.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: ABI-motion groupExperimental treatment 1 intervention
Group B: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Difference in proportion of patients participating in buddy support programs after rehabilitation discharge

Proportion of patients in the ABI-motion group that continues community buddy support after rehabilitation discharge compared with standard care

Time frame
3, 6, 12 months
2

Mean rating of satisfaction with the ABI-motion program

Satisfaction with the ABI-motion program is rated on a rating scale, ranging from 0 (worst) to 10 (best).

Time frame
12 months

Secondary outcomes

1

Change in total minutes of physical activity/week at 6 and 12 months compared with controls

Physical activity is measured with an activity monitor (min/week) and electronic diary

Time frame
0, 6, 12 months
2

Change in Montreal Cognitive Assessment (MoCA) score at 6 and 12 months compared with controls.

The MoCA is a screening tool for detection of mild cognitive impairment. The total score ranges from 0 (worst) to 30 (best).

Time frame
0, 6,12 months
3

Change in functional exercise capacity at 6 and 12 months compared with controls

The 1-minute Sit-to-Stand Test (1mSTS) measures the number of sit-to-stand transitions during 1 minute.

Time frame
0, 6, 12 months
4

Change in Walking Speed at 6 and 12 months compared with controls

10 meter Walk Test (10mWT) assesses walking speed (m/s) over a short duration.

Time frame
0, 6, 12 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Majanka H. Heijenbrok-Kal, PhD

Lead sponsor

Erasmus Medical Center

Sponsor institution

Netherlands Brain Foundation

Collaborator