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SurgeryNCT06585956

Prevent Post-discharge Hospital Admissions Using Mobile Phone App

An observational study of Surgery, run by Cumhuriyet University Hospital at 1 site in Turkey (Türkiye).

Completed

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

Official record
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Trial summary

The investigators aimed to assess the impact of a mobile phone application facilitating real-time visual and verbal communication on reducing emergency room admissions following circumcision. Read more about this study

Who is it for?
Ages 1 year to 15 years, men only
Conditions the study is for
Surgery
What is being tested?
Comminication via Telemedicine and Information
How many people
184 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Apr 2024to 30 Jun 2024
How long will I take part?
3 Months
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 1 year to 15 years
  • Men only
  • No healthy volunteers
  • Child

Study population: Cases of circumcision

Who may be able to join

  • Circumcision

Who cannot join

  • hypospadias
  • cryptoorchidism
  • bleeding diathesis

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Cumhuriyet Univercity

    Sivas, Sivas

Other trials in Turkey (Türkiye)

About this study

Official title: The Role of Physician-Patient Communication Through Mobile Phone Application in Preventing Emergency Room Admissions After Circumcision: a Randomized Prospective Study

The investigators aimed to assess the impact of a mobile phone application facilitating real-time visual and verbal communication on reducing emergency room admissions following circumcision.

Read the detailed description

Today, communication devices make our lives easier and provide convenience in the healthcare sector. Some studies have mentioned that a definitive diagnosis can be made with digital photographs and video images in children with normal findings at the time of examination, and further diagnostic tests become unnecessary . Readmission to the hospital after surgery, especially in children, is a situation that increases the level of anxiety. The use of smart device applications to evaluate both the operation site and functional results after many surgical procedures has reduced the number of re-applications and anxiety levels of patients . Through communication, the patient can articulate their needs to the physician, either verbally or visually, and with the assistance of the physician, navigate through this process much more smoothly. In our randomized prospective study, the investigators aimed to assess the role of a mobile phone application facilitating real-time visual and verbal communication, as well as instant information exchange, in reducing emergency room and urology policlinic admissions due to potential complications after circumcision.

Conditions
Surgery
Being tested
Comminication via Telemedicine, Information
Keywords
Anxiety, Patient Readmission, Circumcission, Telemedicine
Medical subject headings
Anxiety Disorders

What participants receive

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

  • Comminication via TelemedicineBehavioural

    Comminication via Telemedicine With Patients

  • InformationBehavioural

    Informing the patient and their relatives

Study groups in NCT06585956
Study groupRoleWhat they receive
Communication GroupPhysician-Patient Communication Group
Receives: Behavioral: Comminication via Telemedicine
Non-Communication GroupPhysician-Patient Non-Communication Group
Receives: Behavioral: Information

What is being measured

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

  1. The Role of Physician-Patient Communication through Mobile Phone Application in Preventing Emergency Room Admissions after Circumcision: A Randomized Prospective Study

    Predicting reduction in patient readmission rate using telemedicine assistance

    Measured: To estimate the change in the readmission rate during the participants; recovery period (2 months)

Timeline

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

  1. First posted19 Sep 2024
  2. Study start1 Apr 2024
  3. Primary completion30 Jun 2024
  4. Study completion30 Jun 2024

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
Other
Time perspective
Cross-sectional
Enrolment
184 participants (actual)
Target duration
3 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT06585956
Sponsor's protocol ID
SCU-UR-IEE-06
Status last verified
Sep 2024
First submitted
19 Aug 2024
Last updated
19 Sep 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Surgery, run by Cumhuriyet University Hospital at 1 site in Turkey (Türkiye).

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 3 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 19 Sep 2024. 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 Turkey (Türkiye). 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?

The Role of Physician-Patient Communication through Mobile Phone Application in Preventing Emergency Room Admissions after Circumcision: A Randomized Prospective Study (time frame: To estimate the change in the readmission rate during the participants; recovery period (2 months)). 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 19 Sep 2024.

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