AzTrials
AzTrials

Dermatologic DiseasesNCT03913598

Internet and Social Media Use in Dermatology Patients

An observational study of Dermatologic Diseases, run by University Hospital, Basel, Switzerland at 1 site in Switzerland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This study is to assess Internet and social media use in dermatology patients Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Dermatologic Diseases
What is being tested?
patient questionnaire
How many people
650 participants
Where
1 siteSwitzerland
Study dates
21 Mar 2019to 20 Apr 2019
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Outpatients treated at the Department of Dermatology of University Hospital Basel

Who may be able to join

  • Patients treated at the Department of Dermatology of University Hospital Basel

Who cannot join

  • Insufficient knowledge of German language

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • Department of Dermatology, University Hospital Basel

    Basel, 4031

Other trials in Switzerland

About this study

Official title: Internet and Social Media Use in Dermatology Patients - a Survey

This study is to assess Internet and social media use in dermatology patients

Read the detailed description

The Internet and social media bear potential in terms of heath care consumer education, prevention of diseases and dissemination of evidence-based information. The use of the internet and social media platforms both by dermatologists and patients is rapidly evolving. In order to improve the presence and visibility of dermatology-related evidence-based informations on the Internet and in social media, the use and behavior of dermatology patients in this context is studied in more detail.

Being tested
patient questionnaire
Keywords
social media use, online medical services, internet use
Medical subject headings
Skin Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • patient questionnaireOther

    self-administered patient questionnaire regarding the different aspects of internet and social media use in dermatology patients

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Use of the Internet as a source of medical information

    self-administered patient questionnaire regarding motivation to seek for medical information on the Internet

    Measured: single time point assessment at baseline

  2. Use of Social media as a source of medical information

    self-administered patient questionnaire regarding motivation to seek for medical information in Social media

    Measured: single time point assessment at baseline

  3. Duration of Internet/ Social media use by dermatology patients

    self-administered patient questionnaire covering duration of Internet/ Social media use (up to 2 hours/ day; 2 to 4 hours/day; more than 4 hours/day)

    Measured: single time point assessment at baseline

  4. Quality assessment (by patients) of medical information provided

    self-administered patient questionnaire covering quality of medical information provided on the Internet (5 point self-rating scale from very bad to very good)

    Measured: single time point assessment at baseline

  5. Impact of internet/social media on the patient-physician relationship

    self-administered patient questionnaire covering impact of internet/social media on the patient-physician relationship (self-rating scale: positive/ negative/ no impact)

    Measured: single time point assessment at baseline

  6. Previous use of online medical services and online shopping of drugs/medications

    self-administered patient questionnaire assessing previous use of online medical services and online shopping of drugs/medications (yes/ no)

    Measured: single time point assessment at baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Apr 2019
  2. Study start21 Mar 2019
  3. Primary completion20 Apr 2019
  4. Study completion20 Apr 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
650 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03913598
Sponsor's protocol ID
2019-00009; sp19Mueller3
Other IDs
2019
Status last verified
Sep 2019
First submitted
10 Apr 2019
Last updated
18 Sep 2019
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Dermatologic Diseases, run by University Hospital, Basel, Switzerland at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Sep 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Use of the Internet as a source of medical information (time frame: single time point assessment at baseline). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Sep 2019.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in