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Trial Title:
The Effect of Sujok Therapy on Patient Comfort, Pain Intensity, and Anxiety Level in Cancer Patients With Port Catheter Placement
NCT ID:
NCT06430177
Condition:
Cancer
Chemotherapy Effect
Conditions: Official terms:
Pain
Conditions: Keywords:
Su Jok
Pain
Anxiety
Study type:
Interventional
Study phase:
N/A
Overall status:
Not yet recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Supportive Care
Masking:
None (Open Label)
Intervention:
Intervention type:
Behavioral
Intervention name:
Su Jok
Description:
Su Jok will be done
Arm group label:
Experimental
Arm group label:
Placebo
Summary:
Cancer is a fatal disease characterized by uncontrolled growth and proliferation of
tissues and organs in the human body. Among cancer treatments, chemotherapy is the most
commonly used treatment method. The drugs used in chemotherapy cause vascular toxic
effects during administration, frequent blood samples taken from the patient, antibiotic
treatments applied, parenteral nutrition treatments. Subcutaneous venous port catheter
(SCVPK), which is a permanent and long-term vascular access route that can be used for
medical purposes and in emergency situations, is a frequently preferred and safe
intravenous access route because it is not visible outside the body, is well tolerated by
the patient, and has a low risk of infection. However, invasive procedures such as port
needle insertion and replacement can also cause pain, anxiety and changes in vital signs
in patients. Nowadays, the use of non-pharmacological approaches as well as
pharmacological methods is increasing in the management of symptoms such as anxiety
before the invasive procedure and pain during application in patients receiving
chemotherapy treatment. These approaches improve the quality of life of patients and have
a positive physiological effect. One of these approaches is sujok therapy. In Su Jok
application; The reflection points of the organs are on the hands and feet. These points
reflect to the body organ in that area and healing occurs. By finding the right point,
energy flow is provided by massaging with appropriate applicators. This research will be
conducted to examine the effect of Sujok therapy on pain intensity and anxiety level in
cancer patients who have undergone port catheter placement.
The research will be conducted as a randomized experimental and placebo study with a
pretest-posttest control group in the oncology service of Fethi Sekin City Hospital. 90
(30 experimental, 30 control, 30 placebo) cancer patients who accept the research and
meet the sample criteria of the study will be subjected to port catheter application.
Application areas for pain, anxiety and stress before the port catheter to the patients
in the experimental group will be determined with the help of a probe (diagnostic stick),
and seeds will be added to these points approximately 45 minutes before the application
and fixed with a patch. For cancer patients in the placebo group, the same procedure will
be performed with seeds that have a neutral effect on the body. No procedure will be
applied to the patients in the control group. Patient Information Form, General Comfort
Scale (GAS), Visual Analog Scale -Pain (VAS-P), Visual Analog Scale -Anxiety (VAS-A) and
State-Trait Anxiety Scale were used as data collection tools. (DSKÖ) scale will be used.
SPPS 21.0 (Statistical Programme for Social Sciences) package program will be used to
evaluate the data obtained from the research. It is thought that if the objectives of the
study are achieved, it will help reduce the level of pain and anxiety that may occur
during and after port catheter application. In addition, it will contribute to the
professional advancement of the project manager, which is a career development project.
The positive results in this study will guide other interventions to increase the comfort
level of cancer patients who will undergo port catheterization and reduce the level of
pain and anxiety.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- Being over 18 years of age
- Ability to communicate adequately
- Being diagnosed with cancer
- Will receive chemotherapy treatment
- Port catheter placement will be performed
- Suitable for Implantable Port Catheter Placement
Exclusion Criteria:
- Loss of sensation in the hands, amputation, injury, etc. that would prevent
practice. to be
- Patients with chronic pain or anxiety disorders, using any analgesics or anxiolytics
Gender:
All
Minimum age:
18 Years
Maximum age:
85 Years
Healthy volunteers:
Accepts Healthy Volunteers
Locations:
Facility:
Name:
Fırat university
Address:
City:
Elazığ
Zip:
25240
Country:
Turkey
Start date:
June 1, 2024
Completion date:
December 1, 2024
Lead sponsor:
Agency:
Firat University
Agency class:
Other
Source:
Firat University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06430177