Tired! Recharge and re-engage: a program to treat fatigue for youth with Acquired Brain Injury

Tired! Recharge and re-engage: a program to treat fatigue for youth with Acquired Brain Injury - Tired! Recharge and re-engage

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON57313

Enrollment

Registered

2025-02-21

Start date

2024-12-01

Completion date

Unknown

Last updated

2026-03-09

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

Conditions

non-traumatic brain injury Traumatic Brain Injury

Interventions

COGRAT is an existing intervention proven effective in reducing fatigue and will be adapted and made blended for the target group (MOE!)**.

Eligibility

Age

12 Years to 64 Years

Inclusion criteria

Inclusion criteria: - Age 12-19 years, - Must be diagnosed with ABI (traumatic/non-traumatic). - Physically/cognitively sufficiently capable (assessment by rehabilitation physician), - Sufficient knowledge of the Dutch language (for completing questionnaires and following online instructions/modules), - Access to a phone/tablet with internet, - Able to independently complete digital assignments (cognitive and physical training), - Able to come to the rehabilitation center for physical meetings.

Exclusion criteria

Exclusion criteria: Limiting psychiatric disorders

Design outcomes

Primary

Measure	Time frame
Primary study parameter will be: A blended intervention will be delivered to reduce fatigue. The PedsQL* Multidimensional Fatigue Scale (PedsQL*-MFS) will be used as main endpoint to study fatigue pre- and post-intervention.	—

Secondary

Measure	Time frame
Secundary parameters for the pilot intervention will be participation, quality of life, compliance, goal achievement and physical fitness. Parameter (measured by) Participation (Child and Adolescent Scale of Participation (CASP)) Quality of life (PedsQL Generic Core Scales 4.0 (GCS-4.0)) Compliance, training and daily activity levels (Digital monitoring of the progress with Minddistrict/Physitrack) (and an activity tracker that measures active minutes per hour, steps taken per hour, heartrate variability per hour, burneg calories per hour, VO2max per dag and sleeptime per day/night) Goal achievement (Questionnaires at the end (achieved yes/no and program satisfaction)) Physical fitness (6 minute walk test and handheld dynamometry) Goal achievement, feasibility and satisfaction (questionnaires)	—

Measure

Time frame

Secundary parameters for the pilot intervention will be participation, quality of life, compliance, goal achievement and physical fitness. Parameter (measured by) Participation (Child and Adolescent Scale of Participation (CASP)) Quality of life (PedsQL Generic Core Scales 4.0 (GCS-4.0)) Compliance, training and daily activity levels (Digital monitoring of the progress with Minddistrict/Physitrack) (and an activity tracker that measures active minutes per hour, steps taken per hour, heartrate variability per hour, burneg calories per hour, VO2max per dag and sleeptime per day/night) Goal achievement (Questionnaires at the end (achieved yes/no and program satisfaction)) Physical fitness (6 minute walk test and handheld dynamometry) Goal achievement, feasibility and satisfaction (questionnaires)

—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Mar 14, 2026