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The Effect of Mobile Application-Based Education Given to Patients With Tracheostomy on Depression, Social Adaptation and Quality of Recovery

The Effect of Mobile Application-Based Education Given to Patients With Tracheostomy on Depression, Social Adaptation and Quality of Recovery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07337668
Enrollment
45
Registered
2026-01-13
Start date
2025-04-01
Completion date
2025-12-25
Last updated
2026-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tracheostomized Patients, Depression, Social Adaptation, Quality of Recovery

Keywords

mobile application, tracheostomy, education, quality of recovery, depression, social adaptation

Brief summary

The Effect of Mobile Application-Based Education Given to Patients with Tracheostomy on Depression, Social Adaptation and Quality of Recovery

Detailed description

The Effect of Mobile Application-Based Education Given to Patients with Tracheostomy on Depression, Social Adaptation and Quality of Recovery

Interventions

BEHAVIORALMobile application-based education

A structured education program delivered via a mobile application for patients with tracheostomy. The program included educational videos focusing on tracheostomy care, and postoperative recovery. Participants accessed the content throughout the postoperative period in addition to standard care.

Standard postoperative care routinely provided to patients with tracheostomy according to institutional protocols

Sponsors

Saglik Bilimleri Universitesi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged 18 years and older * Patients with a tracheostomy * Able to communicate verbally or in writing * Able to use a smartphone * Provided written informed consent

Exclusion criteria

* Presence of severe cognitive impairment * Presence of severe psychiatric disorder * Patients with neurological diseases affecting swallowing * Inability to use a mobile application * Refusal to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
DepressionBaseline and postoperative 21 daysDepression level was assessed using the Beck Depression Inventory. The Beck Depression Inventory is a 21-item self-report questionnaire used to assess the severity of depressive symptoms. Total scores range from 0 to 63, with higher scores indicating greater severity of depressive symptoms
Social AdaptationBaseline and postoperative 21 daysSocial adaptation was assessed using the Social Adaptation Self-evaluation Scale. The Social Adaptation Self-Evaluation Scale is a self-report instrument designed to evaluate social functioning and adaptation. Total scores range from 0 to 60, with higher scores indicating better social adaptation and functioning
Quality of RecoveryPostoperative 21 daysQuality of recovery was assessed using the Quality of Recovery-40 (QoR-40) questionnaire. The Quality of Recovery-40 is a validated questionnaire assessing postoperative recovery across five dimensions: emotional state, physical comfort, psychological support, physical independence, and pain. Total scores range from 40 to 200, with higher scores indicating better quality of recovery

Secondary

MeasureTime frameDescription
Swallowing FunctionBaseline and postoperative 21 daysSwallowing function was assessed using the Turkish version of the Eating Assessment Tool-10 (T-EAT-10).The Turkish Version of the Eating Assessment Tool-10 is a self-administered questionnaire used to assess symptoms of dysphagia. Total scores range from 0 to 40, with higher scores indicating more severe swallowing difficulties
Oral Care StatusPostoperative 21 daysOral care status was assessed using an oral care assessment tool. Total scores range from 8 to 24, with higher scores indicating poorer oral condition

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026