NCT05688319

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2021

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2021

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 3, 2022

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 5, 2022

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

January 5, 2023

Completed
13 days until next milestone

First Posted

Study publicly available on registry

January 18, 2023

Completed
Last Updated

January 18, 2023

Status Verified

January 1, 2023

Enrollment Period

10 months

First QC Date

January 5, 2023

Last Update Submit

January 17, 2023

Conditions

Keywords

MothersProblems Psychosocial

Outcome Measures

Primary Outcomes (1)

  • Interpersonal Problem Solving Inventory

    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

Study Arms (2)

experimental group

EXPERIMENTAL

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.

Behavioral: Problem-Solving Training

control group

NO INTERVENTION

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.

Interventions

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.

experimental group

Eligibility Criteria

Age18 Years - 65 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • Hearing and speech problems in the mother.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ataturk University

Erzurum, Yakutiye, 25040, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Child Development Disorders, Pervasive

Condition Hierarchy (Ancestors)

Neurodevelopmental DisordersMental Disorders

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

January 5, 2023

First Posted

January 18, 2023

Study Start

August 1, 2021

Primary Completion

June 3, 2022

Study Completion

August 5, 2022

Last Updated

January 18, 2023

Record last verified: 2023-01

Data Sharing

IPD Sharing
Will not share

Locations