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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05544279
Other study ID # 99
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 17, 2020
Est. completion date December 30, 2022

Study information

Verified date September 2022
Source Cukurova University
Contact Dilara Keklik, MSc, RN
Phone +905304565913
Email dkkeklik@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is being conducted in randomized controlled trial design to determine the effect of the education given to the mothers of children with hydrocephalus on caregiver burden and anxiety levels.


Description:

The number of samples to be taken was calculated as a result of the analysis of the scale mean scores in the control group data obtained in the pre-application. At the end of the 3rd measurement, under the assumption that there will be a 20% more decrease in the intervention group compared to the control group, and using the values obtained from the pilot study, it was determined that 20 patients should be included in the experimental and control groups at 5% error, 80% power. Research eligibility criteria were as follows; 1. Having children with hydrocephalus aged 0-1 years 2. Having a child with a ventriculoperitoneal shunt operation indication, 3. Having a child in the preoperative period 4. Being the primary caregiver of the child 5. Being literate 6. Not having another relative with chronical disease to care for 7. Residing in Adana province 8. Mothers who were open to communication and cooperation were included in the study. The hypotheses of the study are as follows; H0: Between the mothers in the control group and the treatment group; H0-1: There is no difference between the groups in terms of Zarit Burden Interview total mean scores. H0-2: There is no difference between the groups in terms of State Anxiety Inventory total mean scores. H03: There is no difference between the groups in terms of Trait Anxiety Inventory total mean scores. H04: There is no relationship between the groups in terms of Zarit Burden Interview and State Anxiety Inventory total mean scores. H05: There is no relationship between the groups in terms of Zarit Burden Interview and Trait Anxiety Inventory total mean scores. Before collecting the data, approvals from the Ethics Board (15 May,2020;99) and from the instituations where the study to be conducted were gained. Besides, principles namely "Informed Consent," "Confidentiality and Protection of Confidentiality," and "Respect to Autonomy" principles were fulfilled by explaining the aim of the study to the participants, by reporting that the information obtained would be kept confidential, and by including the individuals who voluntarily wanted to participate in the study. Zarit Burden Interview, State-Trait Anxiety Inventory and Personal Information Form and Patient Follow-up Form are being used for collecting data. Totally, it was planned to make 7 interviews with the experimental group and 3 interviews with the control group and 3 measurements are made in the experimental and control groups. Data is being collected with the first interview face-to-face and the last interview with the telephone interview technique. Training booklet was assessed by 5 lecturers in the field of Child Health and Diseases Nursing according to a kind of DISCERN measuring instrument- The Suitability of Written Materials Form. As a result of the analysis, the total score obtained from The Suitability of Written Materials Form was found to be 26.2±1.09, which indicates that the readability rate of the training content is also high. Furthermore, as a result of the evaluation of five experts in the field, necessary changes were made in the training material. Training about the content in the booklet and the booklet were given to the experimental group in the first meeting. Each training takes about 45 minutes. Booklets in pdf formats are sent to the control group via whatsApp after the interviews were completed. The content of the training material is topics related to hydracephalus such as what hydrocephalus is, symptoms of hydrocephalus, treatment of hydrocephalus, what shunt is, signs of infection, nutrition and what to do to prevent complications.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 30, 2022
Est. primary completion date October 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: 1. Having children aged 0-1 with hydrocephalus 2. Having a child with a ventriculoperitoneal shunt operation indication, 3. Having a child in the preoperative period 4. Being the primary caregiver of the child 5. Being literate 6. Having no other dependents with chronic diseases at home 7. Residing in Adana province 8. Mothers who were open to communication and cooperation were included in the study. - Exclusion Criteria: 1. Not having 0-1 year old child with hydrocephalus 2. No child in the preoperative period 3. Those who do not undertake the primary care of the child 4. illiterate 5. Having no other dependents with chronic diseases at home 6. Those who do not reside in Adana 7. Not open to communication and cooperation 8. Mothers with hearing and speech disabilities were excluded from the study.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Education
Education is given about the focused disease and its nursing care management

Locations

Country Name City State
Turkey Çukurova University Balcali Hospital Health Education and Research Center Adana Sariçam

Sponsors (1)

Lead Sponsor Collaborator
Cukurova University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Zarit Burden Interview The scale, which is used to evaluate the caregiving difficulties experienced by caregivers of individuals in need of care, was developed by Zarit, Reever, and Bach-Peterson (1980) in 1980. The Turkish validity and reliability study of the scale was carried out by Inci and Erdem (2006). through study completion,1 month
Primary State-Trait Anxiety Inventory (STAI) Spielberger et al. developed it in 1970 and the validity and reliability study of this scale was carried out by Öner and Le Compte in 1977. through study completion, 1 month
Primary Patient Follow-up form The training follow-up form, which was created by the researcher as a result of the literature review, was filled in twice in the 1st week and 1st month after the first interview. The purpose of this form; To determine the educational issues that the mother needs after discharge and to follow up the shunt complications. through study completion, 1 month
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