The Effect of Patient Advocacy Training on Advocacy Skills, Ethical Sensitivity, and Patient Safety Culture in Nurses

ConditionEducation
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorSelcuk University

About this trial

In this study, the aim is to evaluate the effects of patient advocacy training provided to nurses on their advocacy skills, ethical sensitivity, and patient safety culture level.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • measuring knowledge level

    Behavioral

    The study group consists of 70 nurses, each consisting of 35 people. After the routine training of the hospital was given to the control and experimental groups, their consents were obtained and the pre-tests were completed, they were divided into experimental and control groups using simple randomization. The first group of nurses in the control group will not receive any intervention other than the routine training given by the hospital.

  • educational intervention

    Other intervention

    the effectiveness of training by making measurements after training and comparing them with pre-training results

Treatment groups

70 Participants
are divided into 2 treatment groups
Group A: The Effect of Patient Advocacy Training on Advocacy Skills, Ethical Sensitivity and Patient Safety CNo intervention 0 interventions
Group B: Pre-testing was applied to all individuals participating in the study.Active comparator 2 interventions

Trial outcomes

Primary outcomes

1

Patient advocacy scale, Moral sensitivity survey, Patient Safety Culture Hospital Survey

Patient advocacy scale total and sub-dimension scores Moral Sensitivity Questionnaire scale total and sub-dimension scores Evaluation of Patient Safety Culture Hospital Survey is Made Only Based on Positive Response Average Scores

Time frame
up to 8 weeks
2

Patient Advocacy Scale for Nurses, Moral Sensitivity Questionnaire (ADA),Hospital Patient Safety Culture Survey (HSOPSC)

Patient Advocacy Scale for Nurses (HSO) Consists of 39 items and 7 sub-dimensions.- Scoring: Total score ranges from 39 to 195; higher scores indicate higher level of advocacy * Reliability: Cronbach alpha coefficient 0.95; ranges from 0.82 to 0.92 for sub-dimensions Moral Sensitivity Questionnaire (ADA) Consists of 30 items and 6 sub-dimensions,- Scoring: Total score ranges from 30 to 210; lower scores indicate higher ethical sensitivity * Reliability: Cronbach alpha coefficient ranges from 0.82 to 0.84; test-retest correlation coefficient ranges from 0.81 to 0.99 Patient Safety Culture Survey (HSOPSC) * Contains a total of 42 items, assesses patient safety culture in 12 dimensions, Scoring: Each item is assessed using a 5-point Likert scale (1=Strongly disagree, 5=Strongly agree) Reliability: Validity and reliability studies of the Turkish version have been conducted

Time frame
up to 8 weeks

Secondary outcomes

1

Educational intervention

Patient Advocacy Scale for Nurses (HSO) Consists of 39 items and 7 sub-dimensions.- Scoring: Total score ranges from 39 to 195; higher scores indicate higher level of advocacy * Reliability: Cronbach alpha coefficient 0.95; ranges from 0.82 to 0.92 for sub-dimensions Moral Sensitivity Questionnaire (ADA) Consists of 30 items and 6 sub-dimensions,- Scoring: Total score ranges from 30 to 210; lower scores indicate higher ethical sensitivity * Reliability: Cronbach alpha coefficient ranges from 0.82 to 0.84; test-retest correlation coefficient ranges from 0.81 to 0.99 Patient Safety Culture Survey (HSOPSC) * Contains a total of 42 items, assesses patient safety culture in 12 dimensions, Scoring: Each item is assessed using a 5-point Likert scale (1=Strongly disagree, 5=Strongly agree) Reliability: Validity and reliability studies of the Turkish version have been conducted

Time frame
after 8 weeks
2

Post-tests after 8 weeks of training

Pre-tests of Both Groups Comparison of Experimental Group According to Follow-up Times Post-tests of Both Groups Should Also Be Done and Reported

Time frame
1 month

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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