The Effect of Mobile Education on Anxiety and Activities of Daily Living

Not Applicable

Completed

• Conditions: Mobile Education; Anxiety; Postoperative Anxiety; Patient Education; Activities of Daily Living
• Interventions: Other: e-Mobile Application Patient Education for Patients with Thyroidectomy

• Registration Number: NCT05529732
• Lead Sponsor: Cukurova University

Brief Summary

The study was planned as a block randomized controlled experimental study. In order to calculate the sample size needed in our study, a pilot study will be conducted and a priori power analysis will be made based on the results of this study.

E-mobile application will be used as data collection tool. The research will be carried out with 2 groups as application (mobile application) and control (standard care).

Detailed Description

The study was planned as a block randomized controlled experimental study. In order to calculate the sample size needed in our study, a pilot study will be conducted and a priori power analysis will be made based on the results of this study.

E-mobile application will be used as data collection tool. The "E-Mobile Application Training Content Guide" to be integrated into the mobile application will be evaluated by the experts with the "Conformity Evaluation Form of Written Training Materials" and the "DISCERN Scale". After the training content is completed, "Personal Information Form", "STAI State and Trait Anxiety Scale", "Assessment and Monitoring Form for Daily Living Activities" will be used. In the preliminary application, the "System Usability Scale" and the e-mobile application will be evaluated by the patients. The "E-Mobile Application Training Content Guide" created by the researchers in line with the literature will be transferred to the mobile application with the help of computer engineers and graphic designers. Sequence and visuality of education Roper et al. It was designed according to the Life Activities Based Nursing Model developed by The e-mobile application is designed in accordance with the Android operating system and its language is Turkish. Patients who download the application from the virtual market (Google Play) can log in with the user name and password created by the researcher. The user name and password were created by the researcher specifically for each patient during the research process. The number of clicks and the reading time of the topics read by the patients entering the application can be tracked with the help of the created web page. The research will be carried out with 2 groups as application (mobile application) and control (standard care).

Study Timeline

• Study Start: 2021-09-01
• Primary Completion: 2022-03-01
• Study First Submitted: 2022-09-01
• Study First Submitted QC: 2022-09-02
• Study First Posted: 2022-09-07
• Study Completion: 2022-11-21
• Status Verified: 2023-11
• Last Update Submitted: 2023-11-22
• Last Update Posted: 2023-11-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 68

Inclusion Criteria

• Thyroidectomy was planned for benign thyroid disease,
• Hospitalized at least one day before the operation,
• Voluntarily accepted to participate in the study,
• Aged 18 and over,
• Conscious, person-space-time orientation,
• No psychiatric problems,
• No hearing-speech and visual impairment
• who can speak Turkish,
• who underwent partial thyroidectomy/lobectomy/total thyroidectomy under general anesthesia and by the same surgeon,
• who have been using a smartphone for at least one year will be included.

Exclusion Criteria

• Patients with psychiatric problems,
• hearing or speech impairment, who did not approve the informed consent form, who gave up after approval,
• who did not use the mobile application despite using a smartphone,
• who have a profession in the field of health will not be included in the study.
• In addition, patients who did not log into the mobile application, could not be contacted during the research process and whose surgery was canceled for any reason will not be included in the sample.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Application Group	e-Mobile Application Patient Education for Patients with Thyroidectomy	Oral and written consent will be obtained from the patients by face-to-face interview technique at least one day before the surgery. Then, face-to-face interview technique and data collection tools (Personal Information Form and Trait Anxiety Scale) will be applied. It is estimated that the process of obtaining consent and filling out the form will take approximately 5 minutes. The mobile application will be installed on the mobile devices of the patients and the user name and password will be defined by the researcher so that they can log into the mobile application. In the application, a patient warning notification will be sent on the 3rd, 7th and 10th days to remind the patients to fill in the State Anxiety Scale and Daily Living Activities Evaluation and Follow-up Form, which are included in the questionnaires menu and will be active when the day comes.

Primary Outcome Measures

Name	Time	Method
STAI State and Trait Anxiety Inventory:	1 year	STAI State and Trait Anxiety Inventory: The scale was developed by Spielberger in 1964 and adapted into Turkish by Öner and Le Compte. The scale consists of two parts and includes a total of 40 questions. 20 questions in the first part evaluate the state anxiety of individuals, and 20 questions in the second part evaluate the trait anxiety.

Trial Locations

Locations (2)

Muaz GÜLŞEN; 🇹🇷 Adana, Turkey

Muaz Gülşen; 🇹🇷 Adana, Asia, Turkey