NCT07576920

Brief Summary

Anxiety is a state of worry and apprehension caused by internal and external threats. High preoperative anxiety levels have been associated with increased anesthetic requirements, higher morbidity, and mortality rates. In adult patients undergoing various surgical procedures, preoperative anxiety rates have been reported to range from 11% to 80%. Most studies show that postoperative anxiety levels are related to preoperative anxiety levels. In patients undergoing general anesthesia, anxiety levels increase a few days after surgery as issues related to recovery and pain become apparent. Patients with high postoperative anxiety levels have also been reported to have a higher rate of medical complications.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started May 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 29, 2026

Completed
5 days until next milestone

Study Start

First participant enrolled

May 4, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

May 8, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2026

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2026

Completed
Last Updated

June 16, 2026

Status Verified

June 1, 2026

Enrollment Period

2 months

First QC Date

April 29, 2026

Last Update Submit

June 15, 2026

Conditions

Keywords

AnxietyLiver Transplantation

Outcome Measures

Primary Outcomes (1)

  • Anxiety Scores

    The STAI test is a questionnaire comprising two, 20-item scales used to measure state and trait anxiety. The anxiety levels of LLDs will be evaluated by using the STAI. The STAI-State (STAI-S) form will be use to measure the current anxiety level. The test includes questions about how the person feels at that moment. Answers are given on a scale of 4 points. For example: I am calm right now: not at all=1, a little=2, a lot=3, completely=4. The STAI-Trait (STAI-T) form will be use to measure the underlying (ongoing/personality) anxiety level of the patient. The test includes questions about how the person feels in general and is also answered on a scale of 4 points. Each patient will complete these forms preoperatively and postoperatively. The mean (total) score on the STAI has a minimum of 20 and a maximum of 80. The STAI scores are generally classified as no anxiety or low anxiety (score of 20-37), moderate anxiety (score of 38-44), and high anxiety (score of 45-80).

    From 24 hours prior to the operation to postoperative 3. day and 7. day

Secondary Outcomes (2)

  • Presence of an alternative donor

    Prior to the operation

  • Recipient Prognosis

    at the postoperative 3. day and 7. day

Study Arms (1)

Living liver donors

Liver transplant donors who will undergo surgery between May and July 2026

Behavioral: Anxiety scores

Interventions

Anxiety scoresBEHAVIORAL

Anxiety scores will evaluated STAI test. The STAI test consists of two sections of 20 questions each. The first section of the test includes questions about how the person feels at that moment. Answers are given on a scale of 4 points. For example: I am calm right now: not at all=1, a little=2, a lot=3, completely=4. The second section of the test includes questions about how the person feels in general and is also answered on a scale of 4 points.

Living liver donors

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Living liver donors

You may qualify if:

  • ASA 1-2 group patients aged 18-65 years who are liver transplant donors

You may not qualify if:

  • Patients with communication problems, those who are illiterate,
  • Patients do not have sufficient time for the tests,
  • Patients using sedatives, antidepressants, or antiepileptic drugs,
  • Patients with cerebrovascular or psychiatric diseases,
  • Patients with alcohol or substance addiction,
  • Patients who do not want or cannot undergo the second test

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Turgut Ozal Medical Center

Malatya, 44315, Turkey (Türkiye)

RECRUITING

Related Publications (1)

  • Erdogan MA, Ucar M, Ozgul U, Erdogan S, Colak YZ, Ozhan O, Yaman R, Ugur Y, Aydemir S, Parlakpinar H. Preoperative and Postoperative Endogenous Melatonin and Anxiety Levels and Their Correlation in Living Liver Donors. Exp Clin Transplant. 2025 Apr;23(4):278-284. doi: 10.6002/ect.2021.0060. Epub 2021 Jul 16.

    PMID: 34269646BACKGROUND

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

Study Officials

  • Zekine Begeç, professor

    Inonu University Department of Anesthesia

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Zekine Begeç, Professor

CONTACT

Muharrem Uçar, Professor

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof.

Study Record Dates

First Submitted

April 29, 2026

First Posted

May 8, 2026

Study Start

May 4, 2026

Primary Completion

July 15, 2026

Study Completion

July 30, 2026

Last Updated

June 16, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Locations