- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07265401
The Effect of Salutogenic Model-Based Care on Mothers of Children Suffering From Febrile Illness
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Üsküdar
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Istanbul, Üsküdar, Turkey (Türkiye), 34672
- Uskudar University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- The child must have applied to the emergency room with a fever complaint
- Have at least a primary school level education
Exclusion Criteria:
- The child with a fever must be over 5 years old
- Having a psychological disorder
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
While applying the salutogenic care model to the mothers in the experimental group (n=45), a total of three data collection forms were used: the Personal Introduction Form, the Sense of Individual Integrity Scale, and the Coping Attitudes Assessment Scale.
|
Salutogenic Care Model Training Program This is a training program that involves meeting with the salutogenic care model in 3 sessions, providing both fever-related training and completing forms.
|
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No Intervention: Control Group
While routine midwifery care was given to mothers in the control group (n=45) in the service, a total of three data collection forms were used: a Personal Introduction Form, the Sense of Individual Integrity Scale, and the Coping Attitudes Assessment Scale.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
COPE-Coping Attitudes Assessment Scale
Time Frame: 6 months
|
COPE-Coping Attitudes Assessment Scale "Ways of Coping" was developed by Folkman and Lazarus in 1980 and COPE was developed by Carver, Scheier and Weintraub in 1989 (Folkman et al. 1980, Wegner et al. 1987).
Coping Attitudes Assessment Scale is a self-report scale consisting of 60 questions and 15 subscales.
Questions are answered with the options "I never do it" (1), "I occasionally do it" (2), "I do it moderately" (3), "I do it often" (4).
Each of the subscales provides information about a different coping attitude.
The higher the score a person gets from the subscales provides information about which coping attitude the person uses more.
|
6 months
|
|
Outcome Measure
Time Frame: 6 months
|
The Sense of Integrity Scale The Sense of Integrity Scale used in the study was developed by Antonovsky (1987) to measure the abilities of individuals to maintain their health despite stress. The first version of the SOC consists of 29 items on a 7-point Likert-type scale. Eleven items on this scale relate to "understandability," eight items to "meaningfulness," and ten items to "manageability" (Geyer 1997). In 1987, Antonovsky revised the existing SOC scale and developed a shorter version consisting of 13 items. In this short version, five items measure understandability, four items to "meaningfulness," and the remaining four items to "manageability," all on a 7-point Likert-type scale. The scale is a self-report scale consisting of 13 items ranging from 1 to 7. It varies between 13 and 91 points. |
6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Ayça Demir Yıldırım, PhD, Uskudar University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Ü.Ü. Ebe Aslıhan BAŞ
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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