Effect of Short Message Service Use on Anxiety
The Use of an SMS Reminder in Postoperative Medication Compliance in Patients Undergoing Cataract Surgery and Its Effect on Anxiety: A Randomized Controlled Study
1 other identifier
interventional
82
1 country
1
Brief Summary
Background: Paticipants undergoing cataract surgery find postoperative medication management difficult and are anxious about this issue. Differences in the number of medications and frequency of administration can be lead to confusion in participants. Aims and objectives: The aim of this randomized-controlled study was to evaluate the effect of using SMS, which reminds about the intake of medication, on reducing postoperative anxiety in participants undergoing cataract surgery. Design: Randomized controlled study.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jul 2020
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 3, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 8, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
February 8, 2021
CompletedFirst Submitted
Initial submission to the registry
February 25, 2021
CompletedFirst Posted
Study publicly available on registry
March 2, 2021
CompletedMarch 2, 2021
February 1, 2021
7 months
February 25, 2021
February 26, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
postoperative level of anxiety after cataract surgery
The primary point of the study was defined as determining the effect of using SMS, reminding about the intake of medication, on reducing postoperative level of anxiety.
24 months
Secondary Outcomes (1)
Level of patient satisfaction about received message after cataract surgery
24 months
Study Arms (2)
SMS group
EXPERIMENTALAfter postoperative standard discharge education was provided to the patients in the SMS group, they were given an individualized written Postoperative Medication Reference Chart. The patient/relative, whose contact information was received, was informed that they would be reminded via text message (SMS). SMS reminders which were individualized according to the patient based on the doctor's directive, were sent to the patients in the SMS group by the researcher clinical nurse (A. Ş). SMS sending started on postoperative day 1 and ended on day seven. SAI was applied again to all patients who came to the outpatient clinic for control on postoperative day seven. Unlike the control group, the "Patient Satisfaction Form," which was prepared for the use of SMS reminders, was applied to the patients in the SMS group. Confirmation was obtained from the patients and their relatives that SMS reminders were received every day.
Control group
NO INTERVENTIONthe Patient Identification Form and SAI were applied to patients in the control on the day of surgery (postoperative day 0). Routine discharge education was provided to all patients by clinical nurses. During the discharge of the patients in the control group, they were informed about the change of dressing on the next day (postoperative day one) and control in the outpatient clinic on postoperative day seven. The patients were given an individualized written Postoperative Medication Reference Chart indicating the dosage and application time of eye drops they must follow for seven days at home.
Interventions
Eligibility Criteria
You may qualify if:
- Patients who were adults, volunteered to participate in the study, accepted randomization, could communicate in Turkish, had a personal cell phone, could read text messages or were illiterate and had a relative to help them at home after discharge were included in the study.
You may not qualify if:
- Patients did not volunteered to participate in the study and had not a personal cell phone were excluded in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kırklareli University
Kırklareli, 39100, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Figen Dığın, PhD
Kırklareli University, Kırklareli, Turkey
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
February 25, 2021
First Posted
March 2, 2021
Study Start
July 3, 2020
Primary Completion
February 8, 2021
Study Completion
February 8, 2021
Last Updated
March 2, 2021
Record last verified: 2021-02
Data Sharing
- IPD Sharing
- Will not share
There is not a plan to make IPD available.