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Trial Title:
The Effect of Mandala Technique on Acute Nausea-vomiting and Comfort Level in Cancer Patients
NCT ID:
NCT05885126
Condition:
Chemotherapy-induced Nausea and Vomiting
Nursing Caries
Conditions: Official terms:
Nausea
Vomiting
Study type:
Interventional
Study phase:
N/A
Overall status:
Enrolling by invitation
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Intervention model description:
The sample recruited for the research consisted of 38 individuals (19 individuals in the
control group, 19 in intervention group) who were 18 years and older, were receiving a
high emetogenic chemotherapy regimen for the first time, had sufficient fine motor skills
to paint and were volunteering to participate in research. Exclusion criteria were any
physical or mental disability that limited communication or coloring the mandala
template. Homogeneity was ensured by including patients who received chemotherapy regimen
with high emetogenicity. Patient lists numbered according to even and odd numbers were
given in a sealed envelope to a practitioner independent from the researchers.
Primary purpose:
Prevention
Masking:
Single (Participant)
Intervention:
Intervention type:
Other
Intervention name:
MANDALA TECHNIQUE
Description:
The ambient light and the position of the laptop table were adjusted appropriately during
the intervention to help the participants move freely and eliminate the environmental
stimulus. In addition, there was no communication between the patient and the
practitioner during the application.
Arm group label:
Intervention Group
Summary:
Cancer is an important health problem in the world and in our country, and it ranks
second among the causes of death in our country (20.7%). Chemotherapy, one of the most
commonly used methods in cancer treatment, causes many physical and emotional symptoms
while treating the disease. Nausea-vomiting is a common problem in cancer care,
especially in patients receiving chemotherapy.
In the literature, there are studies examining non-pharmacological interventions for the
prevention and management of nausea and vomiting in patients receiving chemotherapy, and
it is seen that the interventions are mostly within the scope of complementary and
alternative approaches. Patients receiving ambulatory chemotherapy may experience
anticipatory nausea in particular, and this is likely to affect the individual's comfort
level. In studies conducted in the field, the comfort level of cancer patients receiving
chemotherapy was determined as moderate.
Today, mandalas are used effectively in the field of art therapy. The possibility of
using mandala in all age groups has contributed to the treatment process of different
diseases and disorders, and its effectiveness has been presented to the scientific world
with many researches around the world. In adults, the mandala has been used both in the
treatment of psychiatric disorders and as a tool to observe the effects of treatments.
Art therapy including mandala drawing has significantly reduced the severity of trauma
symptoms in individuals with anxiety disorders and post-traumatic stress disorder. In the
study of Zhao & Tang (2017) it was determined that mandala drawing therapy reduced the
anxiety of cancer patients.
If the reduction of nausea-vomiting affects the comfort level and the person is relieved,
a more effective treatment environment is created and the quality of life of the person
is increased. In the literature, very limited studies have been reached on the use of the
mandala drawing technique in cancer patients. National and international research
examining the mandala drawing technique, especially in patients receiving ambulatory
chemotherapy, could not be reached. The aim of this study is to determine the effect of
mandala drawing technique on nausea-vomiting and comfort level in patients receiving
ambulatory chemotherapy. It is anticipated that the study to be conducted will contribute
to nursing interventions in the cancer care process and lead to the planning of new
research on the subject.
Detailed description:
This research was planned in a quasi-experimental design with pretest-posttest control
group. It is aimed to determine the effect of mandala technique on nausea-vomiting and
comfort level in patients receiving ambulatory chemotherapy.
For this purpose, the research will be carried out with cancer patients receiving
chemotherapy treatment on an outpatient basis at Gaziantep University Medical Faculty
Training and Research Hospital and Gaziantep University Oncology Hospital between
December 2022 and April 2023. The population of my research will consist of patients who
receive outpatient chemotherapy treatment at Gaziantep University Faculty of Medicine
Oncology Hospital. Individuals who meet the sampling selection criteria from the
specified universe will constitute the sample of the research. Experimental research
requires at least 20 samples. In order for a test to meet the parametric test conditions,
references were made to the sources stating that the groups must have at least 30
individuals. In the research group of our study, it was planned to include 30 application
and 30 control group patients. When these numbers are reached, it is planned to determine
the sample impact power by performing power analysis, and to terminate the research when
at least 80% preferably 100% positive impact power is reached. Randomization of the
sample will be achieved by accepting the first patient who applied to the outpatient
chemotherapy unit randomly and with an appointment at the beginning of the study to the
control group, and the next patient to the experimental group. The patients will be
included in the experimental and control groups in this order until the sample size is
reached.
The implementation of the study will start after the necessary permissions are obtained,
and the application group will be asked to paint the mandalas provided by the researcher
for at least 30 minutes while they are in the chemotherapy unit. The patients will be
given the necessary materials during their stay at home, they will be asked to paint
mandalas at home for 4 days, and the patient will be supported by phone. No treatment
other than standard care will be performed for the control group.
Criteria for eligibility:
Criteria:
Inclusion criteria for the research:
- 18 years of age or older, conscious, literate, not having vision and hearing
problems, being able to communicate verbally,
- Receiving outpatient chemotherapy treatment at Gaziantep University Faculty of
Medicine Training and Research Hospital and Gaziantep University Oncology Hospital,
- Receiving a medium and high emetogenic effective chemotherapy regimen
- Having sufficient fine motor skills to paint,
- Not having any diagnosed psychiatric disorder,
- Agreeing to participate in the research
Exclusion criteria from the study:
- Having any communication problems,
- Having sufficient fine motor skills to paint,
- Refusal to participate in the research.
Gender:
All
Minimum age:
18 Years
Maximum age:
75 Years
Healthy volunteers:
Accepts Healthy Volunteers
Locations:
Facility:
Name:
Gaziantep Islamic and Technology University
Address:
City:
Pazarcık
Zip:
(054) 231-0182
Country:
Turkey
Facility:
Name:
Gaziantep İslamic and Technology University
Address:
City:
Gaziantep
Country:
Turkey
Start date:
December 1, 2022
Completion date:
August 30, 2023
Lead sponsor:
Agency:
Ege University
Agency class:
Other
Source:
Ege University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05885126