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Clinical Trials in Turkey / NCT06670859
Enrolling by invitation Not applicable

The Effect of Mobilization Coverall on Anxiety, Comfort, Physical Privacy and Satisfaction

NCT06670859 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-09-17
Last updated
2025-09-17

Condition(s) studied

Intensive Care UnitMobilityPatient

Investigational drug(s) / intervention(s)

Intervention-Control:Control-Intervention

Intervention-Control:: Patients will complete the STAI before the first mobilization after surgery and then the patients' pain status and the level of anxiety they feel about their physical privacy with the mobilization coverall they will wear during mobilization will be assessed with the VAS.Than,will be asked to perform 4 activities (putting on the coverall-mobilization-sitting in the wheelchair and moving-taking off the coverall) with the overall.Than,will be asked to evaluate the indicator level that they think the coverall they wear protects physical privacy and the levels of comfort and satisfaction they feel about the coverall with the VAS.During the next mobilization,patients will be asked to perform the same application protocol with a traditional hospital gown.Participants who have tried both clothing designs will be interviewed about their experiences using 'interview form' their satisfaction.Than interview,participants will have completed the study by filling out the QUEST 2.0.

Control-Intervention: Patients will complete the STAI before the first mobilization after surgery and then the patients' pain status and the level of anxiety they feel about their physical privacy with the traditional hospital gown they will wear during mobilization will be assessed with the VAS.Than,will be asked to perform 4 activities (putting on the gown-mobilization-sitting in the wheelchair and moving-taking off the gown) with the gown.Than,will be asked to evaluate the indicator level that they think the gown they wear protects physical privacy, and the levels of comfort and satisfaction they feel about the gown with the VAS.During the next mobilization, patients will be asked to perform the same application protocol with the mobilization coverall.Participants who have tried both clothing designs will be interviewed about their experiences using 'interview form' their satisfaction.At the end of the interview, participants will have completed the study by filling out the QUEST 2.0.

Study summary

This study is designed as crossover randomized controlled trial to examine the effect of a mobilization coverall designed for intensive care patients on anxiety, comfort, physical privacy and satisfaction.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Being literate in Turkish * Having undergone a surgical operation * Presence of a urinary catheter after surgery * Presence of Jackson-Pratt and/or Hemovac Drain after surgery * Agreeing to participate in the study Exclusion Criteria: * Patients who cannot be mobilized after surgery * Not completing any phase of the study * Wanting to withdraw from the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kutahya City Hospital Kütahya Turkey (Türkiye)

More Saglik Bilimleri Universitesi trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06670859 on ClinicalTrials.gov ↗ ← All trials in Turkey