- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05405699
'Digitalization in Psychoeducation' The Effect of Tele-Psychoeducation on Problem-Solving Skills and Stress
'Digitalization in Psychoeducation' The Effect of Tele-Psychoeducation on Problem-Solving Skills and Stress: A Randomized Factorial Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The research hypotheses are as follows:
- H1: There is a significant difference between the mean scores of the Problem Solving Inventory in favour of the intervention group in the time series.
- H1: There is a significant difference between the mean scores of the Perceived Stress Scale in favour of the intervention group in the time series.
- H1: The recently developed group tele-psychoeducational intervention is effective for reducing Problem Solving Inventory mean scores.
- H1: The recently developed group tele-psychoeducational intervention is effective for reducing Perceived Stress Scale mean scores.
Research data was collected with an online survey tool (Googledocs) that does not require a usage fee or license. The tool is convenient and economical in that it is suitable for use with any electronic device that can connect to the internet. The developed online form was piloted with ten students. Arrangements were made for the clarity of the questions and the convenience of the online tool. Pilot study data was not included in the findings. The tools detailed below were used to collect the data.
Personal Data Collection Form: This form consists of 11 multiple-choice questions to determine the variables that may have an impact on the sociodemographic characteristics, health history, and problem-solving skills of the participants. The questions were prepared by the research team in the light of the literature.
Problem Solving Inventory: The Problem Solving Inventory (PSI), developed by Heppner and Petersen (1982), is a Likert-type scale, scored between 1 and 6, consisting of 35 items that measure adults' self-perception of problem solving skills. There are items that are reverse coded and excluded from scoring. The higher total scores obtained from the scale indicate that the individual perceives himself as inadequate in terms of problem solving skills. The Cronbach alpha consistency coefficient of the original scale was .90, and the coefficients obtained for the subscales were between .72 and .85. The scale was adapted to Turkish by Şahin et al. (1993), and the Cronbach alpha consistency coefficient was found to be .88. In our study, the Cronbach alpha coefficient was .78.
Perceived Stress Scale: The scale was developed by Cohen et al. (1983), and adapted into Turkish by Eskin et al. (2013). The Perceived Stress Scale (PSS) is designed to measure how stressful situations in one's life are perceived. Five-point Likert-type scale items are interpreted over the total score and two sub-dimensions (Perception of Insufficient Self-efficacy and Perception of Stress Discomfort). A high total score indicates that the person perceives the stress he/she has been loaded with as high; it is interpreted as the methods used in coping with stress are not functional, and therefore they cannot cope with stress effectively. In our study, the Cronbach's alpha coefficient of the scale was determined as .75.
Data Collection: Data collection in the study was planned in line with the Checklist for Reporting Results of Internet E-Surveys (CHERRIES), which can be considered as a method and reporting guide for online survey research. The research's data security was ensured via a user account to which only two members of the research team had access and which would not be shared with any other user, and the access link was terminated when the data collection process was completed.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
İzmir, Turkey
- Ege University Faculty of Nursing
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Being adult
- Being volunteer to participation
- Must be have the required technological opportunities
Exclusion Criteria:
- To receive a professional support that can affect coping skills during the data collection process
- Not participate in 20% of tele-psychoeducational interventions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
|
Problem Solving Approach based problem solving skills psychoeducation's session topics of eight weeks are as follows:
Three days a week for eight weeks, informative posts were shared, asynchronous testing and self-discovery activities were carried out, and a synchronous tele-psychoeducation session was held once a week. Participants were connected to the live broadcast of the research team and interacted via text messages. |
|
No Intervention: Control
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Problem Solving Inventory (first evaluation with posttest)
Time Frame: Through study completion, an average of 4 months
|
The Problem Solving Inventory (PSI), developed by Heppner and Petersen (1982), is a Likert-type scale, scored between 1 and 6, consisting of 35 items that measure adults' self-perception of problem solving skills.
There are items that are reverse coded and excluded from scoring.
The higher total scores obtained from the scale indicate that the individual perceives himself as inadequate in terms of problem solving skills.
The Cronbach alpha consistency coefficient of the original scale was .90, and the coefficients obtained for the subscales were between .72 and .85
(Heppner & Petersen, 1982).
The scale was adapted to Turkish by Şahin et al. (1993), and the Cronbach alpha consistency coefficient was found to be .88.
In our study, the Cronbach alpha coefficient was .78.
|
Through study completion, an average of 4 months
|
|
Perceived Stress Scale (first evaluation with posttest)
Time Frame: Through study completion, an average of 4 months
|
The scale was developed by Cohen et al. (1983), and adapted into Turkish by Eskin et al. (2013).
The Perceived Stress Scale (PSS) is designed to measure how stressful situations in one's life are perceived.
Five-point Likert-type scale items are interpreted over the total score and two sub-dimensions (Perception of Insufficient Self-efficacy and Perception of Stress Discomfort).
A high total score indicates that the person perceives the stress he/she has been loaded with as high; it is interpreted as the methods used in coping with stress are not functional, and therefore they cannot cope with stress effectively.
In our study, the Cronbach's alpha coefficient of the scale was determined as .75.
|
Through study completion, an average of 4 months
|
|
Problem Solving Inventory (second evaluation with follow up)
Time Frame: Through study completion, an average of 7 months
|
Through study completion, an average of 7 months
|
|
|
Perceived Stress Scale (second evaluation with follow up)
Time Frame: Through study completion, an average of 7 months
|
Through study completion, an average of 7 months
|
Collaborators and Investigators
Sponsor
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 (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- EgeTrial2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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