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A Semi-structured Interview PACIENTE Improves Communication With Family Members at the Intensive Care Unit

Result of an Intervention for the Group of Physicians Responsible for Providing Information on the Satisfaction of the Relatives of Patients Hospitalized in an Intensive Care Unit

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02336893
Acronym
PACIENTE
Enrollment
245
Registered
2015-01-13
Start date
2013-08-31
Completion date
2014-08-31
Last updated
2015-01-13

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

Conditions

Communication, Quality of Life

Keywords

Communication Barriers, Total Communication Methods, Quality Improvement, Quality of Health Care, Critical Care

Brief summary

The purpose of this study is to assess whether a formal training strategy using an interview PACIENTE may improve physician's skills and quality of communication with family members at the ICU.

Detailed description

Introduction: Effective communication with physicians is an important factor for families at intensive care unit. Although physicians should have adequate communication skills, training programs are not available that would enable them to enhance this competence. Formal training using a semi-structured interview to improve skills and quality of communication was provided to physicians in charge of supplying information to families at the intensive care unit (ICU). Objective: To assess whether a formal training strategy using an interview PACIENTE may improve physician's skills and quality of communication with family members at the ICU. Methods: A pre- and post- intervention study was designed for a university hospital mixed ICU (medical and surgical). Training was provided to 34 resident physicians in charge of giving information to families at the ICU using interview PACIENTE. The interview was done conjointly with participation in simulated difficult clinical cases with actors posing as family members. Patient registries: Family satisfaction was assessed with a validated survey, FS-ICU 24, in 122 and 123 family members pre- and post-intervention training, respectively, on the fourth day after patient admission to the ICU. The surveys were identified with consecutive numbers and not collected data that would allow subsequent identification of patients or their families. After the intervention, structures of interviews were monitored with checklists designed for this purpose. The meetings were always in the same place for this activity. The surveys were answered on paper and the data included in an SPSS database by one of the researchers. Single questions in the 24-FS-ICU survey were analyzed according to the author's suggestions with minor modifications. Scores from items 1-6 in the published survey were transformed to scores from 0 to 100. The Mann-Whitney U test was used to determine any score differences between pre- and post-interventions. Differences of P\<0.05 were considered statistically significant. The sample size was calculated to be 122 participants for pre-intervention and 122 participants for post-intervention to detect α coefficient of 0.05 and with a power of 0.90. The survey was performed in the waiting room and questionnaires were collected immediately; thus, there were no missing questionnaires.

Interventions

BEHAVIORALTraining

The final training was provided to a group of 34 residents --from internal medicine, anesthesiology, gynecology, and intensive care-- in charge of giving information to the patient's family members in the ICU. They were trained in the semi-structured interview PACIENTE (Present oneself and greet, Attend and listen, Call diagnosis, Inform treatment, Expose prognosis, Name introductory phrases to bad news, Take time to provide empathetic comfort, Explain an action plan involving the family) conjointly while participating in simulated difficult clinical cases with family members-actors. Four training programs were performed from February to September 2014.

Sponsors

Fundación Universitaria de Ciencias de la Salud
Lead SponsorOTHER

Study design

Allocation
NON_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

* That consented to participate in the satisfaction survey * That whom had been in the ICU for 72 h.

Exclusion criteria

* Family members with language barriers (requiring assistance to answer a question in writing) * Previous ICU admission within the study period * Patient's death by the fourth day of admission * Proved reasons for risk of judicial proceedings.

Design outcomes

Primary

MeasureTime frameDescription
Comprehension of the information, measured with the instrument FS-ICU 24. Third question, second part.Four monthsMeasured with the instrument FS-ICU 24. Third question, second part.
Adequate time to address concerns and answer questions, measured with the instrument FS-ICU 24. Tenth question, second part.Four monthsMeasured with the instrument FS-ICU 24. Tenth question, second part.

Secondary

MeasureTime frameDescription
Overall satisfaction with care, measured with the instrument FS-ICU 24.Four monthsMeasured with the instrument FS-ICU 24.
Overall satisfaction with decision-making measured with the instrument FS-ICU 24.Four monthsMeasured with the instrument FS-ICU 24.
Global survey satisfaction measured with the instrument FS-ICU 24.Four monthsMeasured with the instrument FS-ICU 24.

Outcome results

None listed

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