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The Effect of Creative Drama on the Level of Mental Health Literacy

The Effect of Creative Drama Education Applied to Nursing Students on Mental Health Literacy Levels: A Randomized Controlled Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05758155
Enrollment
56
Registered
2023-03-07
Start date
2023-03-01
Completion date
2024-12-01
Last updated
2023-03-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Education, Mental Health Literacy, Nurse's Role

Keywords

nursing educations, mental health literacy, creative drama

Brief summary

This study was planned as a randomized controlled trial to determine the effect of creative drama education given to nursing students on mental health literacy scores

Detailed description

This studies designed experimentally. among the first-year students of nursing who cannot repeat the class, who have not received mental health literacy training before, and who are willing to participate in the study will form the group of the study. The designated group will be divided into experimental (creative drama) and control group (classroom training). Training to the experimental group will be applied to the control group through creative drama through in-f training. The trainings are planned as 4 sessions and each session/lesson is planned as 50+50 (100 minutes). As a measurement tool, the mental health literacy scale will be used as the pre-test and final test.

Interventions

OTHERmental health literacy training supported by creative drama

nursing students will be given two hours of mental health literacy training supported by creative drama one day a week for 4 weeks.

OTHERmental health literacy training supported by classroom instruction

nursing students will be given mental health literacy training supported by two hours of classroom instruction one day a week for 4 weeks.

Sponsors

Abant Izzet Baysal University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Masking description

İn this study, the names of the patients nursing student in the two wards will be sorted and numbered in alphabetical order. After the numbering process, the patients will be selected to the experimental and control group by using the www.randomizer.org/ site by an independent specialist.

Intervention model description

randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Have not received any training on mental health or mental health literacy, Have reached the age of 18 No more class repetition volunteer to participate in the study nursing students were included in the study

Exclusion criteria

Have received any training in mental health or mental health literacy, Under 18 years of age Remaining for class repetition who is not willing to participate in the study nursing students were not included in the study

Design outcomes

Primary

MeasureTime frameDescription
experimental group (creative drama) nursing students' mental health literacy pretest final test scores21 DayMental Health Literacy Scale (RSOS): The scale allows individuals to determine their RSO level and to determine in which areas they may need more support. The scale consists of sub-sub-dimensions of 35 items. The first 15 (1-15) items are quad likert (strongly disagree (1), disagree (2), agree (3), strongly agree (4)) and the next 20 (16-35) items are quintessentially likert (1), disagree (2), disagree (2), agree (3), agree (4), strongly agree (5).
Control group (classroom instruction) nursing students' mental health literacy pretest final test scores21 DayMental Health Literacy Scale (RSOS): The scale allows individuals to determine their RSO level and to determine in which areas they may need more support. The scale consists of sub-sub-dimensions of 35 items. The first 15 (1-15) items are quad likert (strongly disagree (1), disagree (2), agree (3), strongly agree (4)) and the next 20 (16-35) items are quintessentially likert (1), disagree (2), disagree (2), agree (3), agree (4), strongly agree (5).

Countries

Turkey (Türkiye)

Contacts

Primary Contactmakbule TOKUR KESGİN
mtkesgin@gmail.com05555028425
Backup ContactHümeyra Hançer tok
hancertok@gmail.com05446004410

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026