Evaluating the Effectiveness of Art Therapy on Mood, Anxiety, and Pain Levels in Cancer Patients Undergoing Chemotherapy Treatment
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- The effect of art therapy on the cancer patient's pain
研究概览
简要总结
Participants in this research study are asked to tell about their experience with art therapy. Participants in this research study are currently receiving chemotherapy treatment for cancer. The purpose of this study is to learn how art therapy affects mood, anxiety, pain, and emotions of individuals with cancer who are undergoing chemotherapy.
详细描述
In this single-center single-arm non-controlled descriptive study, we aim to describe the effects of a single art therapy session on a cancer patient's mood, pain, anxiety level.
Primary Objectives
- To assess the effect of art therapy on the cancer patient's mood
- To assess the effect of art therapy on the cancer patient's anxiety
- To assess the effect of art therapy on the cancer patient's pain
Secondary Objectives
- To explore differences in response to art therapy by ethnic group, race, age, sex, caregiver support, cancer diagnosis, reason for visit, and marital status
- To explore differences in response to art therapy by primary concern expressed by patients during art therapy sessions
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects are able to give informed consent
- •Any cancer diagnosis
- •Actively undergoing any chemotherapy treatment at Maroone Cancer Center
- •Patients who have never utilized art therapy at Maroone Cancer Center
- •Speaks, reads, and writes in English
- •Able and willing to participate in an art therapy session at Maroone Cancer Center
排除标准
- •Patients without cancer diagnosis
- •Patients not actively undergoing chemotherapy at Maroone Cancer Center
- •Individuals unable to complete art therapy activities independently due to physical and/or mental impairment
- •Under 18 years of age (minors)
- •Patients who have dementia or a legal guardian
- •Unable to speak, read, and write in English
- •Patients who have previously utilized art therapy at Maroone Cancer Center
研究组 & 干预措施
Art Therapy
The art therapy intervention will be executed by an art therapist at the Cancer Center. The same art therapy practices that are utilized in daily practice will be employed in this study. The intervention will include assessment of patient's needs and goals in addition to utilization of various art modalities. Sessions will conclude with processing of the art and supportive counseling as appropriate. Pilot testing of the intervention has been performed informally at Maroone Cancer Center with positive feedback provided by patients and their support systems to the physicians, nurses, and art therapist. Change in pain, emotional distress, depression, adn anxiety will be measured by the emotions thermometer.
干预措施: Emotions Thermometer (Behavioral)
Art Therapy
The art therapy intervention will be executed by an art therapist at the Cancer Center. The same art therapy practices that are utilized in daily practice will be employed in this study. The intervention will include assessment of patient's needs and goals in addition to utilization of various art modalities. Sessions will conclude with processing of the art and supportive counseling as appropriate. Pilot testing of the intervention has been performed informally at Maroone Cancer Center with positive feedback provided by patients and their support systems to the physicians, nurses, and art therapist. Change in pain, emotional distress, depression, adn anxiety will be measured by the emotions thermometer.
干预措施: Art Therapy (Behavioral)
结局指标
主要结局
The effect of art therapy on the cancer patient's pain
时间窗: Change from baseline to after intervention, about 50 minutes
The primary endpoint of the trial is to access the effect of an art therapy session on the patients' mood, anxiety level, and pain. To accomplish this, patients will complete four visual analog scales (VAS) prior to and after the session. The primary end points are the pre-and post session changes in the VAS.
The effect of art therapy on the cancer patient's mood
时间窗: Change from baseline to after intervention, about 50 minutes
The primary endpoint of the trial is to access the effect of an art therapy session on the patients' mood, anxiety level, and pain. To accomplish this, patients will complete four visual analog scales (VAS) prior to and after the session. The primary end points are the pre-and post session changes in the VAS.
The effect of art therapy on the cancer patient's anxiety
时间窗: Change from baseline to after intervention, about 50 minutes
The primary endpoint of the trial is to access the effect of an art therapy session on the patients' mood, anxiety level, and pain. To accomplish this, patients will complete four visual analog scales (VAS) prior to and after the session. The primary end points are the pre-and post session changes in the VAS.
次要结局
- exploratory assessment of the association between sum of pain, anxiety, and mood visual analog scale (VAS) scores and ethnic group of patients(Change from baseline to after intervention, about 50 minutes)
- exploratory assessment of the association between sum of pain, anxiety, and mood visual analog scale (VAS) scores and age of patients(Change from baseline to after intervention, about 50 minutes)
- exploratory assessment of the association between sum of pain, anxiety, and mood visual analog scale (VAS) scores and sex of patients(Change from baseline to after intervention, about 50 minutes)
- exploratory assessment of the association between sum of pain, anxiety, and mood visual analog scale (VAS) scores and cancer diagnosis of patients(Change from baseline to after intervention, about 50 minutes)
- exploratory assessment of the association between sum of pain, anxiety, and mood visual analog scale (VAS) scores and reason for visit of patients(Change from baseline to after intervention, about 50 minutes)
- exploratory assessment of the association between sum of pain, anxiety, and mood visual analog scale (VAS) scores and primary concern expressed by patients during art therapy session(Change from baseline to after intervention, about 50 minutes)
- exploratory assessment of the association between sum of pain, anxiety, and mood visual analog scale (VAS) scores and race of patients(Change from baseline to after intervention, about 50 minutes)
- exploratory assessment of the association between sum of pain, anxiety, and mood visual analog scale (VAS) scores and caregiver support of patients(Change from baseline to after intervention, about 50 minutes)
- exploratory assessment of the association between sum of pain, anxiety, and mood visual analog scale (VAS) scores and marital status of patients(Change from baseline to after intervention, about 50 minutes)