FB PES

Evaluating the Family Buddy Intervention for Vulnerable Population: A Pilot Study of Engagement, Adoption, and Lifestyle Change - FB PES

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON61433

Enrollment

Registered

2026-06-10

Start date

2026-09-01

Completion date

Unknown

Last updated

2026-08-10

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

Conditions

Not applicable. Not applicable.

Interventions

FB prototype&nbsp

Eligibility

Age

16 Years to 99 Years

Inclusion criteria

Inclusion criteria: Able to provide informed consent;Sufficient understanding of the Dutch or English language;Access to a smartphone or tablet;= 16 years of age;

Exclusion criteria

Exclusion criteria: < 16 years of age;Not able to give written informed consent.

Design outcomes

Primary

Measure	Time frame
The main outcomes of this evaluation study are:Change in lifestyle during a 2 months periodChange in mental health between during a 2 months periodActual usage of FB prototype during the 2 month period (frequency and duration)	—

Secondary

Measure	Time frame
Interaction with modules FB prototypeInteraction with features FB prototypePattern of active daysPattern in last log-ins	—

Countries

Netherlands

Contacts

Public ContactA.N. Schonewille - Rosman

Erasmus MC, Universitair Medisch Centrum Rotterdam

familybuddy@erasmusmc.nl010-704 07 04

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Aug 25, 2026