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Study on the Effect of Sensation Awareness Focused Training on the Intervention of Post-ICU Syndrome of Family: A randomized controlled trial

Study on the Effect of Sensation Awareness Focused Training on the Intervention of Post-ICU Syndrome of Family: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102953
Enrollment
Unknown
Registered
2025-05-22
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Post-ICU Syndrome of Family (PICS-F)

Interventions

Intervention group:ICU routine care +SAF-T.Each SAF-T intervention lasted 15-20 minutes and was directed by SAF-T-trained researchers to make them aware of the negative biological stress sensations as
) (40 times per minute), with the amplitude controlled within 90°. During this process, the subjects kept their heads still, tracked the movement of the researchers' fingers only with their eyes, and
Control group:During the hospitalization of ICU patients, briefly introduce the ICU environment, equipment and visiting hours to the family members, maintain good communication with them, promptly con

Sponsors

Affiliated Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) The patient's stay in the ICU is >=24 hours; (2) The age of the patient's family members (parents, children, spouse, brothers or sisters) is =18 years old; (3) Each patient corresponds to one family member, who is responsible for the main care and medical decision-making of the patient. (4) Family members of the patient have no history of mental illness or other serious organic diseases in the past; (5) The family members of the patients gave informed consent and voluntarily participated in this study.

Exclusion criteria

Exclusion criteria: (1) Family members refuse to participate in this researcher due to their own reasons; (2) Those with mental disorders or other serious organic diseases; (3) Researchers with severe hearing and language expression impairments who are unable to cooperate in completing the research.

Design outcomes

Primary

MeasureTime frame
Pressure;Anxiety;Depression;

Secondary

MeasureTime frame
Post-traumatic stress disorder;Sleep;

Countries

China

Contacts

Public ContactYao Li

Department of Respiratory and Critical Care Medicine, Affiliated Hospital of Guizhou Medical University

liyao5452@126.com+86 186 8512 5474

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 15, 2026