Effect of Problem-Solving Training (AtaturkU)

January 17, 2023 updated by: Kübra Gökalp, Ataturk University

Effect of Problem-Solving Training for Mothers With Special Needs Children: A Randomized Controlled Study

The aim of this study, therefore, is to determine the effect of problem-solving training on the interpersonal problem-solving skills of mothers with special needs children. This study was a parallel randomized controlled trial. The mothers were sorted into control and experimental groups (40 experimental and 40 control groups). A personal information form and the Interpersonal Problem Solving Inventory (IPSI) were used to collect data in this research. The participants in the experimental group gived to problem solving training program while the control group was not exposed to any intervention.The data in the control and experimental groups were homogeneously distributed. There was no significant difference in the pre-training test scores for any of the dimensions , but the post-training test scores were significantly higher in the experimental group than in the control group. Intragroup analysis with the Wilcoxon sign-rank test showed that there were significant differences between the pre-training and post-training test scores in the experimental group. Interpersonal problem-solving skills can be improved by providing problem-solving training to the mothers of children with special needs. Based on the findings of this study, it is recommended that psychiatric nurses provide training to protect and improve the well-being of children with special needs and their families.

Study Overview

Detailed Description

Design Data Collection Instruments A personal information form and the Interpersonal Problem Solving Inventory were used to collect data in this research.

Personal Information Form This form was prepared by the researcher, and consists of eight questions that cover the following information: mother's age, mother's education level, income level, family type, number of children, diagnosis of the child with special needs, age of the child with special needs, and gender of the child with special needs.

Problem-Solving Training Program The researchers prepared the content of the training program based on relevant published literature, and the training program has been verified by three experts. The training was conducted by a researcher who is an expert in the field of psychiatric nursing. Before the start of the training, the mothers in the experimental group were taken to the meeting room and were asked to answer a preliminary test. The day and time for the training, which was conducted at the center, were then scheduled. The participants in the experimental group were divided into five groups of eight participants each according to the number of days they visited the center. The training was conducted face to face in the meeting room of the special education and rehabilitation center. Within the scope of the study, problem-solving training was conducted for the mothers in the experimental group in the study once a week for 10 weeks. The duration of each training session was 60-90 minutes. The weekly training sessions for all the experimental groups were completed on the same day.

In the first session of the problem-solving training, the group members met each other, set the rules for the training sessions, and defined the purpose of the meeting. The second and third sessions covered problem orientation, general problem-solving approaches, and alternative solutions. In the fourth and fifth sessions, the importance of recognizing and expressing feelings in real life was discussed. Additionally, the problem-solving styles of the members were discussed, with a focus on whether they had an inattentive, impulsive problem-solving style. In the sixth and seventh sessions, the avoidant style of problem solving, which is a negative problem-solving style, was discussed. Further, participants were asked to reflect on their problem-solving style. In the eighth and nineth sessions, problem-solving dialogue in fictitious and real-life situations was discussed. The skills learned were reviewed through a question-and-answer format. The tenth (and last) session was a general evaluation.

The pre-training test was conducted on the same day in the experimental group and the control group. The control group did not receive any training, and there was no interaction between the experimental group and the control group during the training period. When the training was completed in the experimental group, the post-training test was conducted in both groups of participants on the same day at the center.

Study Type

Interventional

Enrollment (Actual)

80

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Yakutiye
      • Erzurum, Yakutiye, Turkey, 25040
        • Ataturk University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Having a child with special needs
  • Being over the age of 18 years

Exclusion Criteria:

• Hearing and speech problems in the mother.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: experimental group
The participants in the experimental group were divided into five groups of eight participants each according to the number of days they visited the center. The training was conducted face to face in the meeting room of the special education and rehabilitation center. Within the scope of the study, problem-solving training was conducted for the mothers in the experimental group in the study once a week for 10 weeks . The duration of each training session was 60-90 minutes. The weekly training sessions for all the experimental groups were completed on the same day.
Within the scope of the study, problem-solving training was conducted for the mothers in the experimental group in the study once a week for 10 weeks. The duration of each training session was 60-90 minutes.
No Intervention: control group
The control group did not receive any training, and there was no interaction between the experimental group and the control group during the training period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Interpersonal Problem Solving Inventory
Time Frame: 12 week
The inventory was developed by Çam and Tümkaya to measure the interpersonal problem-solving approaches and skills of university students between the ages of 18 and 30 years. The lowest score that can be obtained from the scale is 50 and the highest score is 250. The high score obtained for each subscale indicates that the trait related to interpersonal problem solving is high.
12 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2021

Primary Completion (Actual)

June 3, 2022

Study Completion (Actual)

August 5, 2022

Study Registration Dates

First Submitted

January 5, 2023

First Submitted That Met QC Criteria

January 17, 2023

First Posted (Actual)

January 18, 2023

Study Record Updates

Last Update Posted (Actual)

January 18, 2023

Last Update Submitted That Met QC Criteria

January 17, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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