The Effectiveness of Drawing Interventions

N

National Taipei University of Nursing and Health Sciences

Status

Enrolling

Conditions

Older Adult

Treatments

Other: Drawing Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06197230
NTUNHS_DI

Details and patient eligibility

About

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.

Full 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

Enrollment

128 estimated patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Currently live in nursing home
  2. Have no physical impairment.
  3. Have been staying in nursing home for at least 6 months.
  4. Speak Bahasa Indonesia

Exclusion criteria

  1. Have been diagnosed with psychiatric illness.
  2. Have been diagnosed with severe physical disorders such as advanced cancer or motor impairments

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

128 participants in 2 patient groups

Intervention group ; Drawing Intervention
Experimental group
Description:
The intervention will be applied every week for 6 weeks. The level of depression, resourcefulness, spiritual resourcefulness, and spiritual health will be tested at the first week before the intervention (T0), the 3rd week (T1), the 6th week right after the interventions (T2), 1 month follow-up after the interventions (T3), and 2 months post-intervention.
Treatment:
Other: Drawing Intervention
Control
Other group
Description:
The control group will receive standard care in nursing home
Treatment:
Other: Drawing Intervention

Trial contacts and locations

2

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Central trial contact

Chien Yu Lai, AssProf; Irna Kartina, Master

Data sourced from clinicaltrials.gov

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