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Otorhinolaryngologic DiseasesNCT02453633

Theory Based SMS Reminders - Text's Impact on Patient Attendance

A study testing Emotional SMS text and Standard SMS text in people with Otorhinolaryngologic Diseases and Sleep Disorders, run by Lovisenberg Diakonale Hospital.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The project will be done at the ear, nose and throat outpatient department at Lovisenberg Diakonale Hospital (LDS) in 2015-2016. About 12% of patients with appointments at the surgical outpatient clinic at LDS do not attend their appointment even after receiving both letters and shot message service (SMS) reminders. Read more about this study

Who is it for?
Ages Up to 80 years
What is being tested?
Emotional SMS text and Standard SMS text
Could I receive a placebo?
No, everyone receives an active treatment
How many people
2,000 participants
Where
No sites listed yet
Study dates
May 2015to Aug 2015
Phase
Interventional
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 Up to 80 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Patients (any diagnosis) with a scheduled clinic appointment at the LDS Ear, Nose and Throat Surgical Clinic or scheduled for polysomnography during the inclusion period.
  • Date of birth on or after 01.01.1935

Who cannot join

  • Patients with 2 appointments on the same day, only the first appointment will be included.
  • Patients without a phone number
  • Patients born before 01.01.1935
  • Included patients will not be included again if they get a new appointment in the inclusion period.

Trial locations and contacts

No sites are listed yet.

Trude von Trepka contact

+47 23226862

trvt@lds.no

Grete Saetre contact

+47 23225501

gres@lds.no

About this study

The project will be done at the ear, nose and throat outpatient department at Lovisenberg Diakonale Hospital (LDS) in 2015-2016. About 12% of patients with appointments at the surgical outpatient clinic at LDS do not attend their appointment even after receiving both letters and shot message service (SMS) reminders. Persuasion theory suggests that the SMS reminders may be more effective if the text appeals more to the patient's feelings. The project is designed as a randomized controlled trial in which the control group receives the standard text that has neutral content and the intervention group receives a more emotion-based SMS reminder. The aim is to determine whether the more emotional text reduces the proportion of patients who do not show up for their scheduled appointment at the surgical outpatient clinic.

Read the detailed description

Studies from Norway's Health South East (HSØ) show that the number of patients who do not attend their scheduled appointments account for 200 000 to 250 000 outpatient consultations each year. For comparison, there are 270,000 patients waiting for treatment. It has thus been recommended that regional health authorities take measures to reduce the number of patients who do not attend their scheduled appointment.

This study will evaluate whether short message service (SMS) appointment reminders that appeal to the patient's emotions are more effective for reducing non-attendance to scheduled outpatient appointments at the ear, nose, and throat outpatient clinic at Lovisenberg Diakonale Hospital in Oslo, Norway. The study will be designed as randomized controlled trial in which 2000 patients are randomly assigned to either the intervention group (emotional SMS text) or the control group (standard SMS text with neutral content). Because theory suggests that emotion-based text messages will be more effective reminders, it is hypothesized that they will result in a 50% reduction in the number of patients who do not show for their appointment compared to the control group.

Being tested
Emotional SMS text, Standard SMS text
Keywords
Appointment reminder, Attendance, No-show
Medical subject headings
Otorhinolaryngologic Diseases, Sleep Wake Disorders, Hearing Disorders

What participants receive

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

  • Emotional SMS textOther

    SMS appointment reminder with the following text (translated from Norwegian):

    Reminder about your appointment. There are many who are waiting for treatment. Please notify us if you can not make your appointment on: Tuesday 31 March at 10:00.

    tel. 23225501 or send email to kirpolonh@lds.no later than one weekday prior to your appointment.

    No-show fee: Kr. 640.

    Lovisenberg Diakonale Hospital, Department of Surgery, Ear, Nose and Throat. Do not reply to this message per SMS.

  • Standard SMS textOther

    SMS appointment reminder with the following text (translated from Norwegian):

    Reminder of appointment at Lovisenberg Diakonale Hospital, Department of Surgery, Ear, Nose and Throat: Wednesday 11.feb 2015 at 10:00. For a change, call tel. 23225501 or send email to kirpolonh@lds.no. Do not reply to this message per SMS.

Study groups in NCT02453633
Study groupRoleWhat they receive
Emotional SMS textExperimentalPatients in this arm will receive an emotion-based SMS reminder of their scheduled outpatient clinic appointment.
Receives: Other: Emotional SMS text
Standard SMS textActive comparatorPatients in this arm will receive the standard SMS reminder of their scheduled outpatient clinic appointment.
Receives: Other: Standard SMS text

What is being measured

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

  1. Appointment attendance

    Patient attendance at their scheduled clinic appointment (yes = show up at or before the scheduled time or reschedule at least 24 hours before appointment; no=does not show up by the appointed time).

    Measured: Day of scheduled appointment

Timeline

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

  1. First posted25 May 2015 (estimated)
  2. Study startMay 2015
  3. Primary completionAug 2015 (estimated)
  4. Study completionAug 2015 (estimated)

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
2,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02453633
Sponsor's protocol ID
SMS-ENT
Status last verified
May 2015
First submitted
21 May 2015
Last updated
25 May 2015
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Emotional SMS text and Standard SMS text in people with Otorhinolaryngologic Diseases and Sleep Disorders, run by Lovisenberg Diakonale Hospital.

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 2 inclusion and 4 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: status not confirmed, as of the sponsor's last update on 25 May 2015. Status can change between updates, so confirm with the study contact before making plans.

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?

Results are not available in the source record.

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

Contact Trude von Trepka (+47 23226862, trvt@lds.no), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Appointment attendance (time frame: Day of scheduled appointment). 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 25 May 2015.

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