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Can an app improve patients' knowledge of their medical condition and treatment options?

Assessing the efficacy of an educational smartphone or tablet app with subdivided and interactive content to increase patients’ medical knowledge: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN98629372
Enrollment
188
Registered
2018-05-13
Start date
2017-04-01
Completion date
Unknown
Last updated
2019-04-29

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

Conditions

Knee osteoarthritis Musculoskeletal Diseases

Interventions

A surgeon-blinded randomized controlled trial was conducted with 213 patients who were referred to one of the six Dutch hospitals by their general practitioner owing to knee complaints that were indic

Sponsors

Interactive Studios
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Referred by GP to orthopedic surgeon for suspected knee osteoarthritis 2. Fluent in Dutch 3. Possess an email address and a smart phone or tablet 4. At least 10 days between scheduling the appointment and the hospital visit were required, to give patients in the app group the chance to experience the intervention

Exclusion criteria

Exclusion criteria: 1. Not Dutch-speaking 2. Not in possession of smartphone or tablet

Design outcomes

Primary

MeasureTime frame
Patients' knowledge (perceived and actual) about their illness and the treatment options. Actual knowledge was measured 2 days prior to the consultation by a 12-item multiple choice questionnaire, with possible scores ranging from 0 to 36. Perceived knowledge was also measured 2 days before the consultation by a 5-item multiple choice questionnaire, with possible scores ranging from 0 to 25.

Secondary

MeasureTime frame
1. Satisfaction with information and patient knowledge was measured 2 days before the consultation by using NRS scores ranging from 0 to 10 2. Certainty of the treatment chosen was measured 1 day after the consultation using an NRS 0 to 10 scale.

Countries

Netherlands

Contacts

Public ContactThomas Timmers
thomas@interactivestudios.nl0031 73 644 6069

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 23, 2026