Ignite Creation Date:
2024-05-06 @ 7:57 PM
Last Modification Date:
2024-10-26 @ 3:17 PM
Study NCT ID:
NCT06197230
Status:
RECRUITING
Last Update Posted:
2024-01-09
First Post:
2023-12-26
Brief Title:
The Effectiveness of Drawing Interventions
Sponsor:
National Taipei University of Nursing and Health Sciences
Organization:
National Taipei University of Nursing and Health Sciences
Study Overview
Official Title:
The Effectiveness of Drawing Interventions on Depression Levels Resourcefulness and Spiritual Health of Older Adults in Nursing Homes
Status:
RECRUITING
Status Verified Date:
2023-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The study will consist of two stages The first stage of the study expects to find associations within dependent variables depression level resourcefulness spiritual resourcefulness and spiritual health in older adults The second stage estimated that art drawing interventions will be effective for improving depression levels resourcefulness spiritual resourcefulness and spiritual health
Detailed Description:
A cross-sectional research design will be used in the first stage and the second stage of the research will be an intervention and longitudinal study with a randomized control trial design In the first stage four instruments will be applied such as the Geriatric Depression Scale GDS Resourcefulness Scale RS Spiritual Resourcefulness Scale SpRS and Spiritual Screening Tool for Older Adults SSTOA to measure the levels of depression resourcefulness spiritual resourcefulness and spiritual health of older adults at nursing homes in Indonesia Three hundred older adults will be recruited through purposive sampling in the first stage of the study while 128 participants will be recruited and randomized and assigned to both the experimental and control groups There will be 64 subjects in each group The art drawing intervention will be applied and last for 6 weeks in the experimental group Five times of examinations about the related variables will be performed at the first week before intervention implemented T0 the second measure will be performed 3 weeks after the intervention started T1 6 weeks of drawing intervention the third examine will be tested T2 and 1 and 2 months after the intervention completed the participants will be asked to test for the T3 and T4
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None