We expect that, compared to a standard text-only, a leaflet with pictograms leads to better perceived comprehensibility, utility and design quality of the leaflet by consumers. This could lead to better recall and understanding of the drug…
ID
Bron
Aandoening
Hypertension; (health) literacy
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The main study parameter is change in blood pressure
control between baseline and the first standard control measurement compared between the control and intervention group.
Doel van het onderzoek
We expect that, compared to a standard text-only, a leaflet with pictograms leads to better perceived comprehensibility, utility and design quality of the leaflet
by consumers. This could lead to better recall and understanding of the drug information, increasing patients’ self-efficacy, and in turn intention to adhere and actual adherence, which could lead to better blood pressure control. Additionally, we aim to gain insight into the
question as to whether such intervention is especially beneficial for low-literate people, who are not sufficiently helped with a text-only leaflet format.
Onderzoeksopzet
Blood pressure control means that the patient has achieved the target blood pressure that was set out by their treating physician. Values at baseline (last measurement by HCP before first prescription of
antihypertensive drugs) will be compared to blood pressure measurements of the first routine check-up (usually three weeks after start of medication).
The secondary outcomes will be measured during two interviews - one at t=2-3 weeks and one at t=4-5 weeks after the patients have received the leaflet in the pharmacy.
Onderzoeksproduct en/of interventie
The control group will receive a secondary patient information leaflet that is text-only; the intervention group will receive the same information with pictograms added.
Publiek
M.M. van Beusekom
Sylviusweg 72
Leiden 2333 BE
The Netherlands
071 527 1886
m.m.van_beusekom@lumc.nl
Wetenschappelijk
M.M. van Beusekom
Sylviusweg 72
Leiden 2333 BE
The Netherlands
071 527 1886
m.m.van_beusekom@lumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Adult patients who get prescribed antihypertensive medication for the first time, or for the first time after at least a year of not having received this medication.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
A potential subject who meets any of the following criteria will be excluded from participation in this study:
- unable to verbally communicate in Dutch
- blind
- under 18 years of age
- incapacitated
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL5593 |
NTR-old | NTR5699 |
Ander register | : P15.209 |