CClinicalTrials.gg
CompletedNCT01399970TeleacneUpdated Jan 14, 2014

Use of Mobile Teledermatology in the Care of Acne Patients

An interventional study of Mobile Teleconsultation Arm (MTA) and Outpatient Consultation Arm (OCA) in Acne, sponsored by Medical University of Graz. Completed at 1 site in Austria. Open to participants aged 12 Years to 30 Years. Per ClinicalTrials.gov, last updated 2014-01-14.

Sponsored by Medical University of Graz · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
69
Allocation
Randomized
Ages
12 Years to 30 Years
Sex
All
01

Study summary

The purpose of the present study is to determine whether a mobile teledermatology care model can achieve better clinical outcomes as compared to conventional, outpatient care for the management of severe acne treated with isotretinoin.

The superiority of mobile care in comparison to conventional, outpatient care will be investigated regarding

  1. effectiveness: Global evaluation Acne (GEA) score -response at week 24
  2. safety: drop out rates and medication side effects
  3. overall patient satisfaction with acne care and therapy
  4. overall physician satisfaction with mobile acne care
02

Conditions studied

  • Acne

Browse trials for

Keywords

  • Mobile Teledermatology
  • Telemedicine
  • Acne
03

In context

Acne Vulgaris

730 studies on the registry are indexed under Acne Vulgaris; 86 are open to participants now.

This study's enrollment of 69 is close to the median of 69 across 628 interventional studies indexed under Acne Vulgaris.

Browse Acne Vulgaris studies →

Lead sponsor

Medical University of Graz is the lead sponsor of 459 studies on the registry; 98 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Female or male, aged 12 to 30 years

  • with facial acne
  • requiring systemic isotretinoin treatment (GEA-Score: 3-5)
  • with basic handy skills
  • with a signed consent form

Exclusion criteria

Exclusion Criteria:

  • Pregnancy or lactation period
  • Withdrawal of informed consent
  • Non-compliance, failure to comply with protocol requirements
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
69 participants (actual)

Study arms

  • Other
    Outpatient Consultation Arm (OCA)

    Conventional in Office Care

    Other: Outpatient Consultation Arm (OCA)

  • Experimental
    Mobile Teleconsultation Arm (MTA)

    Mobile Teledermatology Care

    Other: Mobile Teleconsultation Arm (MTA)

Interventions

  • OtherMobile Teleconsultation Arm (MTA)

    In addition to a face-to-face visit at baseline, patients will conduct "mobile visits" at home every two weeks. The general practitioner of choice will perform examinations, such as laboratory or occasionally pregnancy tests every 4 weeks according to the treatment guidelines.

    Also known as: MTA, Health Care Service Modality

  • OtherOutpatient Consultation Arm (OCA)

    Patients will receive routine outpatient care at the clinic according to the treatment guidelines, and will be scheduled for outpatient visits every 4 weeks.

    Also known as: OCA, Health Care Service Modality

06

What researchers measure

Primary outcomes

  1. Global evaluation Acne score (GEA)

    Change from Baseline in the median GEA score at week 24

    Time frame: week 24

07

Study locations

1 site
  • Department of Dermatology, Medical University of Graz
    Graz, 8036, Austria
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 14, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01399970
Lead sponsor
Medical University of Graz
Collaborators
National Bank of Austria
Responsible party
Rainer Hofmann-Wellenhof, MD (Prof. Dr., Medical University of Graz) — Principal investigator
First posted
Jul 22, 2011
Start date
Apr 2011
Primary completion
Dec 2012
Completion
Jan 2013
Last update
Jan 14, 2014

Study contacts

Rainer Hofmann-Wellenhof, MD
study director · Department of Dermatology, Medical University of Graz

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2014. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion