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Clinical Trials in Turkey / NCT07735351
Starting soon Not applicable

Sandplay-Act. Older: Structured Sandplay Activity for Older Individuals

NCT07735351 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-08-17
Last updated
2026-08-19

Condition(s) studied

Healthy AgingElderly (People Aged 65 or More)

Investigational drug(s) / intervention(s)

Sandplay-Act. Older: Structured Sandplay Activity for Older IndividualsControl

Sandplay-Act. Older: Structured Sandplay Activity for Older Individuals: Sandplay-Act Older (Structured Sandplay Activity for Older Individuals) is a structured sandplay activity developed to support older individuals in expressing their emotions, thoughts, and life experiences symbolically. The intervention consists of structured sessions where participants create scenes in a sand tray using miniature figures and make sense of their life experiences through these scenes. The program will be conducted twice a week for a total of four sessions. Each session will last approximately 60 minutes.

Control: Participants in the control group will not participate in structured sand play activities during the study period. Participants will continue with the institution's routine care and social activities; however, no psychosocial interventions will be applied within the scope of the study.

Study summary

This research was planned to determine the effect of structured sandplay activities on positive and negative affect and levels of meaning in life in elderly individuals. The research will be conducted as a single-blind, randomized controlled trial with a pre-test, post-test design at the Gül Kokulu Çınarlar Vefa Konağı of the Isparta Municipality Health Affairs Directorate between July 2026 and July 2027. Prior to the research, ethical committee approval and institutional permission for implementation will be obtained. The research population consists of 400 individuals registered with the institution. The sample will consist of 60 individuals (30 in the intervention group and 30 in the control group) who meet the inclusion criteria, are selected using block randomization, and provide informed consent. The control group will receive no intervention; a pre-test will be administered on the first day, and a post-test will be administered on the day the intervention for the experimental group ends. The intervention group will participate in sandplay activities twice a week for a total of four sessions; a pre-test will be administered on the first day, and a post-test will be administered in the last session. Data collection is planned for the period between July 2026 and July 2027 using the Personal Information Form (PIF), the Positive-Negative Affect Scale (PANAS), and the Meaning in Life Scale (MLS). Data will be analyzed using the SPSS (Statistical Program for Social Sciences) statistical analysis package, and statistical significance will be accepted at p \< 0.05.

Eligibility

Sex
ALL
Min age
65 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Voluntary participation in the study * No specific condition that would cause learning difficulties (auditory or visual perception disorders, etc.) * Being between 65-80 years of age * No acute psychiatric disorder or severe cognitive impairment Exclusion Criteria: * Having a mental or physical disability that prevents communication and attendance at sessions (inability to speak, diagnosis of severe dementia, etc.)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Suleyman Demirel University Isparta Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07735351 on ClinicalTrials.gov ↗ ← All trials in Turkey