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The Effect of Art-Based Intervention on Fatigue, Anxiety, Perception of Nurse Presence, and Quality of Life in Patients With Hematological Cancers

The Effect of Art-Based Intervention on Fatigue, Anxiety, Perception of Nurse Presence, and Quality of Life in Patients With Hematological Cancers

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07551817
Enrollment
52
Registered
2026-04-27
Start date
2026-05-01
Completion date
2026-12-31
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Art-based Intervention, Fatigue, Hematological Cancer, Nurse Presence, Quality of Life

Keywords

Art-based intervention, Hematological cancer, Nurse presence, Quality of life, Fatigue, Anxiety

Brief summary

This study will be conducted in a randomized controlled experimental design to examine The effect of art-based intervention on fatigue, anxiety, perception of nurse presence, and quality of life in patients with hematological cancer. The study will be conducted with 52 patients (26 intervention, 26 control groups) treated in the Hematology department of a training and research hospital between May 2025 and October 2026. Art-based intervention will be applied to the intervention group for 2 week (3 sessions per week), No application will be made to the control group. The data collection tools in the study are the Patient Identifier Information Form, Cancer Fatigue Scale, Functional Assessment of Cancer Therapy-General Scale (FACT-G), Hospital Anxiety and Depression Scale (HADS), and Nurse Presence Scale (PONS).

Interventions

OTHERart-based intervention

The Art-Based Intervention program will be implemented in 3 sessions per week, for a total of 6 sessions. Before starting the Art-Based Intervention program, the researcher will provide information about the purpose of the activity and the tools to be used. Each session will have a theme, and the session will be conducted according to the instructions given to the patient within the framework of this theme. Before each session, the theme specific to that day will be explained to the patients. Sessions will last approximately 45 minutes.

Sponsors

Gazi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Being between 18 and 65 years of age * Speaking and understanding Turkish * Being literate * Having a diagnosis of hematological cancer, * Receiving chemotherapy in an inpatient ward, * Not having a psychiatric diagnosis, * Having an ECOG score of 1 or 2,

Exclusion criteria

* Having vision loss and hearing loss, * Having an ECOG score of 3 or 4 * Patients who wanted to leave the study * Failure to attend at least two sessions of art therapy.

Design outcomes

Primary

MeasureTime frameDescription
Functional Assessment of Cancer Therapy-General Scale (FACT-G)0 st day (before intervention); 14 st day (after intervention) and 28 st day (after intervention).It is a system based on health-related quality of life measurements. FACT-G consists of four sub-dimensions and 27 items: physical condition, social life and family condition, emotional condition, and activity status. The sub-dimension scores of the 27-item, five-point Likert-type scale are evaluated as follows: none: 0, very little: 1, somewhat: 2, quite: 3, very much: 4. The score ranges are 0 to 28, 0 to 28, 0 to 24, and 0 to 28 for the physical condition, social life and family condition, emotional condition, and activity status subscales, respectively. The maximum total score that can be obtained from the scale is 108, and the minimum score is 0.
Cancer Fatigue Scale0 st day (before intervention); 14 st day (after intervention) and 28 st day (after intervention).This 5-point Likert-type scale consists of three sub-sections: physical, emotional, and cognitive, totaling 15 items. The highest possible score is 28 for the physical dimension, 16 for the emotional dimension, and 16 for the cognitive dimension, for a total of 60 points.
Hospital Anxiety and Depression Scale (HADS)0 st day (before intervention); 14 st day (after intervention) and 28 st day (after intervention).Designed to assess patients' mental health and take necessary precautions. It is a 14-item, 4-point Likert-type scale. Each item has a different score. Items 1, 3, 5, 6, 8, 10, 11, and 13 show decreasing severity and are scored as 3, 2, 1, 0; items 2, 4, 7, 9, 12, and 14 are scored as 0, 1, 2, 3. For anxiety, patients scoring between 0-10 are interpreted as having no anxiety, and those scoring 11 and above are interpreted as having anxiety. For depression, patients scoring between 0-7 are interpreted as having no depression, and those scoring 8 and above are interpreted as having depression.
Nurse Presence Scale0 st day (before intervention); 14 st day (after intervention) and 28 st day (after intervention).The scale measures nurse presence with 26 items and patient satisfaction with the last two items. Each item is scored as follows: never (1 point), rarely (2 points), sometimes (3 points), frequently (4 points), and always (5 points). An increase in the score indicates that the nurse's presence and the behaviors she provides are increasing, and patients perceive this positively.

Countries

Turkey (Türkiye)

Contacts

CONTACTOzlem Canbolat
ozlemcanbolat@gazi.edu.tr+90 312 216 26 86

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 28, 2026