This Study Evaluates the Effect of Artistic Activities on Anxiety, Spiritual Well-being, Hope, and Vital Signs in Abdominal Surgery Patients
Conditions
Keywords
Abdominal Surgery, Spiritual Well-being, Art Therapy
Brief summary
The surgical process can cause high levels of anxiety and stress in patients, and abdominal surgery is particularly anxiety-provoking due to the risk of severe pain and complications. Artistic activities can be an effective complementary method for reducing anxiety and improving mental well-being and hope levels in individuals. Studies have shown that activities such as music therapy and visual arts have positive effects on pain, anxiety, and vital signs in surgical patients. This randomized controlled trial aims to evaluate the effects of artistic activities on anxiety, spiritual well-being, hope, and vital signs in patients undergoing abdominal surgery. The research will be conducted on patients undergoing abdominal surgery at the Department of General Surgery at Dokuz Eylül University. The data collection tools used will be the "Patient Assessment Form," "Vital Signs Form," "Visual Analog Anxiety Scale," "Spiritual Well-Being Scale," and "State Hope Scale." The intervention group will participate in mandala coloring as an artistic activity, while the control group will perform breathing exercises. Data analysis will be conducted using the SPSS 29.0 software package. Descriptive and analytical statistics will be used in the data analysis. The results of the study will determine the effect of artistic activities performed on abdominal surgery patients in the preoperative period on anxiety, spiritual well-being, hope, and vital signs. Based on the effectiveness of preoperative artistic activities in clinical use, a decision will be made as to whether they are useful in preparing patients for surgery in the preoperative period.
Interventions
BEHAVIORALArt activities
In the study, pre-tests and post-tests were administered to patients in the experimental and control groups by the first researcher in the patients' rooms. The pre-test data for the study will be collected using the "Patient Diagnosis Form," "Vital Signs Form," "Visual Analog Anxiety Scale," "Spiritual Well-Being Scale," and "State Hope Scale" through face-to-face interviews lasting an average of 10 minutes. After the data is collected, the experimental group will participate in art activities from the body and mind therapy group, while the control group will perform breathing exercises. Final test data will be collected 10 minutes after the activities are completed.
BEHAVIORALbreathing exercises
the control group will perform breathing exercises
Sponsors
Dokuz Eylul University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Be 18 years of age or older * Be scheduled to undergo elective abdominal surgery (stomach, esophagus, colorectal, hepatobiliary) * Be conscious and able to communicate * Be willing to participate in the study
Exclusion criteria
* Patients requiring emergency abdominal surgery * Patients with chronic psychiatric disorders * Patients with severe cognitive impairment * Patients with severe hearing or vision loss * Patients requiring intensive care * Patients with degenerative brain disorders
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| anxiety | Baseline (pre-test), before the intervention - assessed once immediately prior to the intervention. | Anxiety levels will be measured using the Visual Analog Anxiety Scale (VAAS). The scale ranges from 0 to 10, where 0 indicates no anxiety and 10 indicates the highest possible anxiety. Higher scores represent worse anxiety. The baseline (pre-test) measurement will be obtained during a face-to-face interview prior to the intervention. |
| Spiritual Well-Being | Baseline (pre-test), before the intervention - assessed once immediately prior to the intervention. | Spiritual well-being will be assessed using the Spiritual Well-Being Scale.It was developed by Daaleman and Frey (2004), and its Turkish validity and reliability study was conducted by Serbest and Şahin (2022). The scale consists of 12 items and two subscales (self-efficacy and life plan). Participants' responses are rated on a 5-point Likert-type response scale ranging from 1 = "Strongly agree" to 5 = "Strongly disagree." The total score of the scale ranges from 12 to 60. The baseline (pre-test) measurement will be obtained during a face-to-face interview prior to the intervention. |
| State Hope | Baseline (pre-test), before the intervention - assessed once immediately prior to the intervention. | Hope levels will be assessed using the State Hope Scale. The scale consists of six items. Responses were collected using an 8-point Likert scale (1= Strongly disagree, 4= Somewhat disagree, 8= Strongly agree). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Vital signs | Baseline (pre-test), before the intervention-assessed once immediately prior to the intervention. | Vital signs will be assessed using the Patient Vital Signs Form, which includes blood pressure, pulse, respiratory rate, temperature, and pain level. Measurements will be obtained following standard clinical procedures during the baseline (pre-test) assessment prior to the intervention. Values will be interpreted according to established physiological reference ranges, and higher pain scores represent worse symptoms. |
Countries
Turkey (Türkiye)
Contacts
PRINCIPAL_INVESTIGATORNazife Gamze Özer Özlü, Phd
Dokuz Eylul university Nursing Faculty
Outcome results
None listed