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Evaluation of the guideline evidence-based health information in combination with a training programme for providers of health information

Effect of a complex intervention comprising the guideline evidence-based health information and training programme on the quality of health information: study protocol of a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN96941060
Enrollment
150
Registered
2019-03-07
Start date
2019-03-15
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Evidence-based health information Not Applicable

Interventions

Participants in the intervention group receive the guideline evidence-based health information and an adjunctive training programme, which is intended to facilitate the appropriate use of the guidelin

Sponsors

German Aerospace Center (DLR)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Institutions or working groups (up to 10 members) responsible for the production and publishing of information material. 2. Have published any information in the last eighteen months. 3. At least a single information produced in the last three years has to fulfil the following criteria: 3.1. Has to inform a health-related decision. 3.2. Has to address patients or medical laypersons. 3.3. Has to discuss different options regarding one specified health problem. 3.4. Does not inform about a single option, procedure or healthcare system and it does not give general advice on health and wellbeing.

Exclusion criteria

Exclusion criteria: 1. Members of the working groups on the guideline evidence-based health information or the GPGI are not eligible. 2. Produce exclusively (drug) fact(s) boxes 3. Offer exclusively counselling services such as medical online consulting websites, health-related blogs, forums or communities and (online) encyclopaedias.

Design outcomes

Primary

MeasureTime frame
The quality of health information material produced by the participants using the instrument MAPP’INFO (MAPPin health INFOrmation quality). Quality is assessed after the production process has been finished and not later than 12 months. Quality is operationalised as the extent of compliance with the recommendations of the “Guideline for evidence-based health information”.

Secondary

MeasureTime frame
Assessment is carried out along with the primary outcome by comparing the extent of compliance with the recommendations of the “Guideline for evidence-based health information”: 1. Whether information about possible benefits is provided in an appropriate manner. 2. Whether information about possible harm is provided in an appropriate manner. 3. In the case of diagnostic problems: whether information about the reliability and safety of the test is provided in an appropriate manner. 4. The neutrality of the wording/language of the health information. 5. Whether the health information target group has been involved in the development process using appropriate methods.

Countries

Austria, Germany, Switzerland

Contacts

Public ContactJulia Lühnen
julia.luehnen@medizin.uni-halle.de0049 345 557 1220

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 27, 2026