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Pilot Study for the Validity of a Content-based Information Provision Tool Aimed at Improving the Hospitalization Experience of Liver Transplant Patients

Pilot Study for the Validity of a Content-based Information Provision Tool Aimed at Improving the Hospitalization Experience of Liver Transplant Patients

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06424808
Enrollment
40
Registered
2024-05-22
Start date
2024-05-21
Completion date
2024-11-30
Last updated
2024-05-22

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

Conditions

Inpatients, Liver Transplantation

Brief summary

The investigators aim to evaluate the improvement of the inpatient experience and the usability of a content-based tool (a brochure). This involves consolidating video content for inpatients on a single website and providing access to it via QR codes in a brochure format. \[Patients\] Considering this as a pilot study, the investigators plan to recruit around 30 participants. Both the experimental and control groups will receive standard care and information, with the experimental group additionally receiving the brochure. Random assignment will be used for the experimental and control groups. Surveys and interviews will be conducted to assess changes in patient experience and usability before and after providing the brochure. \[Medical Staff\] Among the medical staff involved in the liver transplant surgical process, researchers will select participants based on their degree of involvement with the intervention subjects. After obtaining their consent, interviews will be conducted concerning patient experiences and the brochure.

Interventions

OTHERConsolidating content on a single website and providing access to it via QR codes in a brochure format

The group assigned to the experimental group will receive information in the same manner as current patients do, with the addition of receiving a brochure once when moving to a general ward after surgery. Afterward, they are free to use the brochure. The control group will receive information only in the manner currently provided to patients.

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

\[Patients\] * Adults aged 18 and over * Patients who are scheduled to undergo or have undergone liver transplant surgery * Recruited through a call for research participants and have consented to participate in this study \[Medical Staff\] * Adults aged 18 and over * Medical staff at Samsung Medical Center involved in the post-liver transplant treatment process

Exclusion criteria

\[Patients\] * Individuals who have not consented to participate in this study * Individuals whose health condition makes it difficult to participate in the intervention * During the research period, the researcher will check if the brochure content has been shared during surveys or interviews with the research participants (information dissemination). If information dissemination is confirmed, the participant will be excluded from the study. \[Medical Staff\] * Individuals who have not consented to participate in this study * Medical staff not involved in the liver transplant treatment process

Design outcomes

Primary

MeasureTime frameDescription
Inpatient Experience 1During the interventionInpatient Experience Evaluation Score, which ranges from a minimum of 0 to a maximum of 100 points, with higher scores indicating better patient experiences.
Inpatient Experience 2During the interventionAnalysis of survey response trends and frequencies between the experimental and control groups
Inpatient Experience 3Patient: During the intervention and after intervention(Two times)/Medical staff: During the study periodQualitative research through interviews

Secondary

MeasureTime frameDescription
Informational value of the intervention toolDuring the interventionAsking informational value of the intervention tool from survey and interview
Areas for improvementDuring the interventionA survey and interview on the advice for improvement
Usability value of the intervention toolDuring the interventionSurvey uses 'System Usability Scail' which ranges a minimum of 0 to a maximum of 100 points, with higher scores indicating better usability. Also related question will be asked by intervew.
Regarding utilization of the intervention toolDuring the interventionA survey and interview on the experience of utilization during hospitalization

Contacts

Primary ContactSu Min Kim, Ph.D
flyhighsoom@gmail.com821020340550

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026