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Enrolling by invitation NCT07631260

The Efficacy of ICU Diary on Sleep, Fatigue and Stress

No phase Interventional Sleep

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: ICU diary.
Who it may be relevant to
Registry conditions: Sleep. Basic parameters: from 20 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Taiwan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

The Effect of Constructive ICU Diary on Stress, Sleep Disturbances and Fatigue of Primary Family Caregiver in ICUs

Overview

To create a constructive ICU diary and to comprehend the effect of Constructive ICU Diary on Stress, Sleep Disturbances and Fatigue of Primary Family Caregiver in ICUs.

Interventions

  • Other ICU diary
    ICU diary

Primary outcome measures

  • sleep disturbance [Time frame: baseline and one week later]
  • fatigue severity [Time frame: baseline and one week later]
  • stress [Time frame: baseline and one week later]
  • Coping [Time frame: baseline and one week later]
  • Social Support [Time frame: Multidimensional Scale of Perceived Social Support (MSPSS) The MSPSS is a 12-item self-report instrument that assesses perceived support from three sources: family, friends, and significant others, with four items in each subscale (Chou, 2000; Zimet et]

Eligibility criteria

Inclusion criteria

  • caregivers who has ICU patients using ventilators for more than 48 hours

Exclusion criteria

  • sleep disturbance history

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Prevention

Study locations

Taiwan · 1 center
  • Taichung Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation — Taichung

Identifiers

NCT: NCT07631260 · REC112-21

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗