NCT05665933|Unknown
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Sponsor study identifier
interventional
60
1 country
2
Study Start
December 1, 2022
Actual (reported)Primary Completion
December 15, 2022
Actual (reported)Study Completion
July 2023
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
The aim of this study is to evaluate the effect of acceptance and commitment therapy-based psychoeducation on test anxiety, study skills and psychological flexibility on adolescents. test anxiety scale, study skills scale and psychological flexibility scale are data collection tools. The pretest-posttest is a randomized controlled trial. Experimental and control groups were formed. A 6-week psychoeducation will be applied to the experimental group.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
July 2023
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
December 1, 2022
Actual (reported)December 7, 2022
Actual (reported)December 15, 2022
Actual (reported)December 27, 2022
Actual (reported)July 2023
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Change of Exam Anxiety Scale Total Score
Change in test anxiety scale at the end of 6 weeks. The highest score from the test anxiety scale is 80 and the lowest score is 20. A high score defines high anxiety.
6 weeks
Change study skills in adolescents.
Change in test study skills scale.A maximum of 165 and a minimum of 55 points are obtained from the study skills scale. A high score defines the ability to study effectively.
6 weeks
Change the level of psychological flexibility
6 weeks
PSYCHOEDUCATION PROGRAM Total Duration: 6 Weeks Session Duration: 90 min Frequency: 1 day per week Number of People: 30
Similar training will be provided after the study is completed. Number of People: 30
Total Duration: 6 Weeks Session Duration: 90 min Frequency: 1 day per week Number of People: 30
Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.
ArtvinCoruhU
Artvın, Center, Turkey (Türkiye)
ArtvinCoruhU
Artvın, Turkey (Türkiye)
Kübra Tan
https://www.artvin.edu.tr/kubra-tan
First Submitted
December 7, 2022
First Posted
December 27, 2022
Study Start
December 1, 2022
Actual (reported)Primary Completion
Contact the study team to confirm eligibility.
December 15, 2022
Actual (reported)Study Completion
July 2023
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Last Updated
January 5, 2023
Record last verified: 2023-01
The name and results of the study will be shared.
Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.
Source: ClinicalTrials.gov.
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