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Sandplay Activity in Psychiatry Clinic (SAPC)

Not Applicable
Completed
Conditions
Sandplay Therapy
Anxiety
Registration Number
NCT05073289
Lead Sponsor
Akdeniz University
Brief Summary

This research was conducted to examine the effect of sandplay activity on anxiety and well-being levels in patients in psychiatric clinics.

The research was carried out in Isparta Süleyman Demirel University Psychiatric Clinic as a single-blind randomized controlled experimental study in the pre-test, final-test order between 2020-2021. Ethical permission was obtained from the Clinical Research Ethics Committee and application permission from the institution for pre-research. 63 patients (intervention-32 and control-31) selected by block randomization method formed the universe of the study. No intervention was applied to the control group. A preliminary test and a final test were performed two days apart, one hour apart on the first and fourth days. Two sessions of sandplay activity were applied to the intervention group with a decongest of two days, and each session was pre-tested. The data was collected using "The Personal Information Form", "The Spielberger Status Anxiety" inventory, and "Well-Being Star Scale" and also data showed normal distribution. In statistical analysis, T-Test, Chi-Square Test, pearson correlation test was used dependent and independent groups.

For the purpose of the research, the hypotheses of the research are as follows::

1. Hypothesis (H1): after intervention, anxiety levels of patients who underwent sandplay activity (in a psychiatric clinic) are lower than in the control grouproup

2. Hypothesis (H1): after intervention the level of well-being of patients undergoing sand play activity (in a psychiatric clinic) is higher than that of the control group.

3. Hypothesis (H1): there is a negative correlation between the level of anxiety and the level of well-being in psychiatric clinics who sandplay activity is practiced and not practiced.

This research is Turkish language.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
64
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
"Well-being Star Scale"4 days changes after the first interview
"Spielberger Status Anxiety Inventory"4 days changes after the first interview
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Sema Soysal

🇹🇷

Isparta, Merkez, Turkey

Sema Soysal
🇹🇷Isparta, Merkez, Turkey

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