Stress and Satisfaction Levels of Mothers According to Neuman's Systems Model on Stress and Satisfaction Levels of Mothers With Children in the Intensive Care Unit and Effective Decision Making

NCT06429592 | Not Yet Recruiting

• 1 other identifier: gulsahogulerciyes4023640013
• Study Type: observational
• Target: 40
• Locations: 0 countries
• Sites: N/A

Brief Summary

Research; It will be carried out to examine the effect of the empowerment program structured according to the Neuman systems model on the stress and satisfaction levels and effective decision-making of mothers whose children are in the intensive care unit.

Conditions

Nurse-Patient Relations

Keywords

Mother; Pediatric intensive care; Effective decision making; Satisfaction; Stres

Outcome Measures

Primary Outcomes (1)

• Mothers' stress levels and satisfaction levels will be evaluated.

  For mothers in the experimental group, data will be collected with data collection tools after acceptance of admission to the intensive care unit. The prepared strengthening program will be applied for a total of 5 days starting from the first day of hospitalization. While the treatments are being carried out to the mothers, no other treatments will be performed in the unit. Different time slots will be scheduled for each experiment. After the 5th day of the application is completed, data will be collected with data collection tools and mothers' stress levels and satisfaction levels will be evaluated.

  3 months

Study Arms (2)

experimental group

Data collection tools for mothers in the experimental group after acceptance of admission to the intensive care unit \[Descriptive Characteristics Form, Parental Stress Scale: (Pediatric Intensive Care Unit), Empowerment of Parents in The Intensive Care (EMPATHIC-30) (Empowerment of Parents in Intensive Care Scale), Decision Data will be collected using the Conflict in Making and Decision Making Confident Scale (KVÇS and KEOÖ). The prepared strengthening program will be applied for a total of 5 days starting from the first day of hospitalization. While the mothers are being treated, no other treatment will be done in the unit. Different time slots will be scheduled for each experiment. After the 5th day of the application was completed, data collection tools were used.

Other: education

control group

Data collection tools from mothers in the control group after admission to the intensive care unit \[Descriptive Characteristics Form, Parental Stress Scale: (Pediatric Intensive Care Unit), Empowerment of Parents in The Intensive Care (EMPATHIC-30) (Empowerment of Parents in Intensive Care Scale), Decision Data will be collected using the Conflict in Making and Decision Making Confident Scale (KVÇS and KEOÖ). The routine operation of the intensive care unit will continue and data will be collected again after 5 days of hospitalization.

Other: education

Interventions

education OTHER

nursing care practice

control group; experimental group

Eligibility Criteria

• Age: 18 Years+
• Sex: female
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Mothers who want to voluntarily participate in the research

You may qualify if:

• Communicable,
• Mothers whose children are admitted to the intensive care unit,
• Mother must be over 18 years old
• The child has a biological mother
• Mothers who agreed to participate in the study and signed written consent forms,
• The child's intensive care stay must be at least 5 days.

You may not qualify if:

• Wanting to leave the study,
• The child must have left the intensive care unit less than 5 days ago,
• The mother is under 18 years of age.

Sponsors & Collaborators

• TC Erciyes University: lead

MeSH Terms

Conditions

Personal Satisfaction

Interventions

Educational Status

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Socioeconomic Factors; Population Characteristics

Study Officials

• oznur basdas, professor

  erciyes universitesi

  STUDY DIRECTOR

Central Study Contacts

GULSAH OGUL

CONTACT

6177507711; gulsahogul@gmail.com

Study Design

• Study Type: observational
• Observational Model: CASE CONTROL
• Time Perspective: PROSPECTIVE
• Target Duration: 5 Days
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: May 20, 2024
• First Posted: May 28, 2024
• Study Start: May 17, 2024
• Primary Completion: September 15, 2024
• Study Completion: October 15, 2024
• Last Updated: May 28, 2024

Record last verified: 2024-05