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Effect of Solution-Focused Support Program on Anxiety Levels of Parents During the COVID-19 Pandemic

Primary Purpose

Anxiety, Parents, Covid19

Status

Completed

Phase

Not Applicable

Locations

Turkey

Study Type

Interventional

Intervention

Solution-Focused Support Program

About this trial

This is an interventional supportive care trial for Anxiety focused on measuring anxiety, child, nursing practice, parents, Solution-Focused Support Program

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Parents with children aged 3-6,
Having internet at home or mobile phone,
Parents who volunteer to participate in the study

Exclusion Criteria:

Having communication problems,
Parents who have not attended at least one session

Sites / Locations

Online- Data will be collected through the form created with the Google-Forms

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

intervention group

control group

Arm Description

Solution-Focused Support Program will apply to the participants.

No intervention will be applied to the parents in the control group.

Outcomes

Primary Outcome Measures

State-Trait Anxiety Inventory (STAI)

STAI was developed by Spielberg et al. In 1970 to measure the trait and state anxiety levels of individuals and was adapted to Turkish by Öner and Le Compte (1983) (Gilik and Avşaroğlu 2017). There are a total of 40 questions in the State-Trait Anxiety Scale. The State Anxiety Sub-Scale (STAI-S) evaluates how an individual feels at a particular time and under certain conditions. The Trait Anxiety Subscale (STAI-T) generally assesses how an individual feels. The scores obtained from both scales vary between 20 and 80. High score indicates high anxiety level, low score indicates low anxiety level.

Secondary Outcome Measures

Full Information

NCT ID

NCT04609722

First Posted

October 26, 2020

Last Updated

February 4, 2023

Sponsor

Adiyaman University Research Hospital

1. Study Identification

Unique Protocol Identification Number

NCT04609722

Brief Title

Effect of Solution-Focused Support Program on Anxiety Levels of Parents During the COVID-19 Pandemic

Official Title

Effect of Solution-Focused Support Program on Anxiety Levels of Parents With Children Aged 3-6 Years During the COVID-19 Pandemic

Study Type

Interventional

2. Study Status

Record Verification Date

February 2023

Overall Recruitment Status

Completed

Study Start Date

July 1, 2020 (Actual)

Primary Completion Date

December 1, 2020 (Actual)

Study Completion Date

April 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Principal Investigator

Name of the Sponsor

Adiyaman University Research Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

5. Study Description

Brief Summary

In this research, it was aimed to determine the anxiety levels of parents in the Covid-19 pandemic and to examine the effects of the Solution-Focused Support Program, which is planned to be given to parents with high anxiety levels.

Detailed Description

The study is conducted with parents whose children aged 3-6 years, and have high anxiety levels. In collecting research data; an introductory information form prepared by researchers and the State-Trait Anxiety Inventory will be used.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Anxiety, Parents, Covid19

Keywords

anxiety, child, nursing practice, parents, Solution-Focused Support Program

7. Study Design

Primary Purpose

Supportive Care

Study Phase

Not Applicable

Interventional Study Model

Parallel Assignment

Masking

Participant

Allocation

Randomized

Enrollment

90 (Actual)

8. Arms, Groups, and Interventions

Arm Title

intervention group

Arm Type

Experimental

Arm Description

Solution-Focused Support Program will apply to the participants.

Arm Title

control group

Arm Type

No Intervention

Arm Description

No intervention will be applied to the parents in the control group.

Intervention Type

Other

Intervention Name(s)

Solution-Focused Support Program

Intervention Description

All participants will be given a program of 4 sessions for 4 weeks. Each session is planned to last approximately 50 minutes.

Primary Outcome Measure Information:

Title

State-Trait Anxiety Inventory (STAI)

Description

Time Frame

5 minutes

10. Eligibility

Sex

All

Minimum Age & Unit of Time

18 Years

Maximum Age & Unit of Time

45 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: Parents with children aged 3-6, Having internet at home or mobile phone, Parents who volunteer to participate in the study Exclusion Criteria: Having communication problems, Parents who have not attended at least one session

Overall Study Officials:

First Name & Middle Initial & Last Name & Degree

Ceyda Başoğul

Organizational Affiliation

Adiyaman University

Official's Role

Principal Investigator

First Name & Middle Initial & Last Name & Degree

Emriye Hilal Yayan

Organizational Affiliation

İnönü University

Official's Role

Principal Investigator

First Name & Middle Initial & Last Name & Degree

Mürşide Zengin

Organizational Affiliation

Adiyaman University

Official's Role

Principal Investigator

Facility Information:

Facility Name

Online- Data will be collected through the form created with the Google-Forms

City

Adıyaman

ZIP/Postal Code

02100

Country

Turkey

12. IPD Sharing Statement

Plan to Share IPD

Learn more about this trial

Effect of Solution-Focused Support Program on Anxiety Levels of Parents During the COVID-19 Pandemic

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