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(Cost)effectiveness of the Intervention 'Gezond En Goed Met Elkaar' (GGME)

V

VU University of Amsterdam

Status

Enrolling

Conditions

We Are Not Studying a Disease or Condition
The Study is Focused on People with Limited Health Literacy

Treatments

Behavioral: Gezond en goed met elkaar

Study type

Interventional

Funder types

Other

Identifiers

NCT06644547
2024.0213

Details and patient eligibility

About

The goal of this intervention study is to learn if the intervention can increase positive health and health literacy in people with limited health literacy. The main questions it aims to answer are:

  • Does participating in the intervention 'Gezond en goed met elkaar' increase participant's positive health?
  • Does participating in the intervention 'Gezond en goed met elkaar' improve health literacy?

Researchers will compare people who participate in the intervention with people who haven't participated in the intervention yet.

Participants will:

  • participate in the intervention (3 months)
  • fill out questionnaires every 3 months

Enrollment

120 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 years or older

Exclusion criteria

  • analfabetism
  • insufficient language level of Dutch to be able to participate in the intervention

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

120 participants in 3 patient groups

Intervention 'Gezond en goed met elkaar'
Experimental group
Description:
see description of the intervention 'Gezond en goed met elkaar'
Treatment:
Behavioral: Gezond en goed met elkaar
Control group
No Intervention group
Description:
Participants do not receive the intervention yet. They have to wait 3 months before they start with the intervention. They will fill out questionnaires at baseline, 3, 6 and 9 months.
Control group 2
No Intervention group
Description:
Participants do not receive the intervention yet. They have to wait 6 months before they start with the intervention. They will fill out questionnaires at baseline, 3, 6 and 9 months.

Trial contacts and locations

1

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Central trial contact

Iris Koelmans, MSc

Data sourced from clinicaltrials.gov

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