- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05658367
Effect of Aromatherapy Massage on Pain and Anxiety After Mastectomy
Effect of Massage Made With Aromatherapy Oil After Mastectomy on Acute Arm Pain and Anxiety: a Randomized Controlled Study
Study Overview
Status
Conditions
Detailed Description
Breast cancer ranks first among the most common cancers in women in Turkey, and one out of every four women diagnosed in 2014 was breast cancer (Turkish Ministry of Health Public Health Institution, Turkey Cancer Statistics, 2017). Breast cancer is considered both a local and systemic disease. In the planning of the treatment, the decision of surgery is made by considering the stage of cancer, and the most frequently applied intervention is mastectomy, which involves the partial or complete removal of the breast tissue (Turkish Ministry of Health, General Directorate of Health Services. Breast Cancer Prevention, Screening, Diagnosis, Treatment, and Follow-up Clinical Guide, 2020; Tola et al., 2021). It is stated that in patients who have undergone breast surgery, especially during axillary lymph node dissection, due to the possibility of intercostobrachial nerve injury, pain, numbness, and weakness may be felt in the chest wall, arm, and shoulder in the postoperative period, acute/chronic, neuropathic and phantom pain, lymphedema may develop (Ozmen, 2012; Nemli et al., 2017). Post-operative pain decreases in the first few days, but in some patients, the severity of pain does not decrease or even increase despite post-operative pain management (Mc Mahon et al., 2013). Anxiety experienced by patients in the preoperative period, including breast cancer patients, is an important factor in the level of pain intensity felt after surgery (Stamenkovic et al., 2018; Kulkarni et al., 2017). Effective anxiety and acute pain management are important in terms of shortening the recovery period of the individual, reducing the treatment costs, preventing the occurrence of chronic pain, and increasing the quality of life. For this reason, it is mentioned that non-pharmacological methods can be used in addition to pharmacological treatment to assist treatment (Chou et al., 2016; Small and Laycock, 2020; Reisli et al., 2021). Today, it is known that aromatherapy has an important place among complementary and holistic therapy methods (Zor et al., 2021). However, it is stated that the studies on aromatherapy massage are weak in terms of evidence and more studies should be done on this subject (Ayik and Ozden, 2018). It is stated that aromatherapy oils are applied by inhalation method alone rather than applied with massage, there are few studies on the effectiveness of massage with aromatic oils, therefore more studies on aromatherapy massage should be done in the treatment of pain, anxiety, and depression (Crosby, 2018; Raffi, 2020).
It is seen that studies conducted after breast surgery are mostly focused on the development of chronic pain rather than acute pain intensity after surgery (Kulkarni et al., 2017). In the literature, the effects of aromatherapy massage on anxiety and acute pain severity in patients who are planning for breast surgery are examined, foot reflexology or classical massage (Dion et al., 2015) according to the massage area preferred by the patient in the postoperative period, classical massage applied to the chest region in the preoperative period (Dion et al., 2015). Xiao et al., 2018) there is research on interventions.
No clinical study was found that evaluated the severity of acute pain and anxiety level in the arm after Simple Mastectomy (SM) / Modified Radical Mastectomy (MRM) surgery with sesame oil, sesame-lavender oil mixture, and aromatherapy massage applied in the postoperative period. Therefore, the result of this study is important because it forms the basis for a clinical study.
With the results to be obtained from the research; It is aimed at better understanding the effects of these herbal-based agents in aromatherapy treatment, contributing to nurses' non-pharmacological treatment interventions, and providing quality care in the management of anxiety and acute pain in patients, and thus to provide new information to evidence-based nursing practices.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul, Turkey (Türkiye), 34396
- Sisli Etfal Training and Research Hospital
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Eyalet/Yerleşke
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Istanbul, Eyalet/Yerleşke, Turkey (Türkiye)
- Sisli Etfal Training and Research Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion criteria;
- 18 years and over,
- literate,
- Agreeing to participate in the study,
- Person, place, and time orientation,
- Visual (except for those with better vision using a visual aid), auditory communication difficulties (except for those with better hearing ability using a hearing aid) that will prevent them from understanding the information given and expressing the pain situation correctly,
- No speech impediment/communication problem,
- Simple mastectomy (BM) and modified radical mastectomy (MRM) were performed,
- Not using any TAT method,
- Able to use technology (smartphone, computer, etc.),
- Individuals with technology devices (smartphone, tablet, computer, etc.)
Exclusion criteria;
- Not speaking Turkish and illiterate in Turkish,
- Those who are allergic to the oils to be used in the massage during the application,
- Involved in a different study conducted in the clinic,
- Breast prosthesis placed during surgery,
- Having physical and cognitive problems at a level that cannot apply massage,
- Individuals diagnosed with mood disorders (using any medication for depression, panic attacks, dysthymia, or bipolar disorder)
- Transferred to the intensive care unit in the postoperative period,
- Severe bleeding, hematoma, seroma, nerve injury, or lymphedema developing in the postoperative period,
- Developing an allergy to the oils to be used in the massage during the application,
- Those who want to leave work voluntarily,
- Individuals who do not comply with the working process and conditions will be excluded from the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Group 1
- Group I: The group applied arm massage with sesame oil
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After the surgery, 3 hours after the painkiller application, the patients will massage their arms with sesame oil for 15 minutes with classical massage manipulations.
Other Names:
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Experimental: Group 2
- Group II: The group applied arm massage with a mixture of sesame-lavender oil
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After the surgery, 3 hours after the painkiller application, the patients will massage their arms with sesame- lavender oil mixed for 15 minutes with classical massage manipulations.
Other Names:
|
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Placebo Comparator: Group 3
- Group III (Control): The group applied arm massage with paraffin oil
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After the surgery, 3 hours after the painkiller application, the patients will massage their arms with paraffin oil for 15 minutes with classical massage manipulations.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in NUMERICAL PAIN SCALE (NUMERİCAL RATING SCALE- NRS)
Time Frame: In the postoperative period, the patient's pain is recorded at 08:00 and 08:30, 20:00 and 20:30 with analgesic application, and at 11:00, 11:15 and 23:00 and 23:15 with massage application.
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It is based on the expression of pain intensity in numbers.
In numerical scales, 0 points define the absence of pain, while the value of the number increases as the severity of pain increases, and 10 points indicate unbearable pain
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In the postoperative period, the patient's pain is recorded at 08:00 and 08:30, 20:00 and 20:30 with analgesic application, and at 11:00, 11:15 and 23:00 and 23:15 with massage application.
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|
STATUS ANXIETY SCALE
Time Frame: Instant anxiety data of the patient are recorded in the postoperative period, at the 15th minute after the massage.
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It is a 20-item scale used to measure the instantaneous anxiety level of individuals.
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Instant anxiety data of the patient are recorded in the postoperative period, at the 15th minute after the massage.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
VITAL FINDINGS REGISTRATION FORM
Time Frame: In the postoperative period, the patient's body temperature is recorded 0 minutes before the analgesic, 30 minutes after the analgesic, 0 minutes before the massage and 15 minutes after the massage.
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It is the form that includes the patient's body temperature.
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In the postoperative period, the patient's body temperature is recorded 0 minutes before the analgesic, 30 minutes after the analgesic, 0 minutes before the massage and 15 minutes after the massage.
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ANALGESIC FOLLOW-UP FORM
Time Frame: Data are taken from the patient's file during the hospitalization for 2 days.
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In this form, information about the name, type, number/dose, route of administration and frequency of analgesic administered in the postoperative period is included.
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Data are taken from the patient's file during the hospitalization for 2 days.
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VITAL FINDINGS REGISTRATION FORM
Time Frame: In the postoperative period, the patient's pulse is recorded 0 minutes before the analgesic, 30 minutes after the analgesic, 0 minutes before the massage and 15 minutes after the massage.
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It is the form that includes the patient's pulse.
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In the postoperative period, the patient's pulse is recorded 0 minutes before the analgesic, 30 minutes after the analgesic, 0 minutes before the massage and 15 minutes after the massage.
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VITAL FINDINGS REGISTRATION FORM
Time Frame: In the postoperative period, the patient's respiratory is recorded 0 minutes before the analgesic, 30 minutes after the analgesic, 0 minutes before the massage and 15 minutes after the massage.
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It is the form that includes the patient's respiratory.
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In the postoperative period, the patient's respiratory is recorded 0 minutes before the analgesic, 30 minutes after the analgesic, 0 minutes before the massage and 15 minutes after the massage.
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VITAL FINDINGS REGISTRATION FORM
Time Frame: In the postoperative period, the patient's blood pressure is recorded 0 minutes before the analgesic, 30 minutes after the analgesic, 0 minutes before the massage and 15 minutes after the massage.
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It is the form that includes the patient's blood pressure.
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In the postoperative period, the patient's blood pressure is recorded 0 minutes before the analgesic, 30 minutes after the analgesic, 0 minutes before the massage and 15 minutes after the massage.
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
NUMERICAL PAIN SCALE (NUMERİCAL RATING SCALE- NRS)
Time Frame: The patient's pain is recorded in the preoperative period.
|
It is based on the expression of pain intensity in numbers.
In numerical scales, 0 points define the absence of pain, while the value of the number increases as the severity of pain increases, and 10 points indicate unbearable pain
|
The patient's pain is recorded in the preoperative period.
|
|
STATUS ANXIETY SCALE
Time Frame: Instant anxiety data of the patient are recorded in the preoperative period.
|
It is a 20-item scale used to measure the instantaneous anxiety level of individuals.
|
Instant anxiety data of the patient are recorded in the preoperative period.
|
|
VITAL FINDINGS REGISTRATION FORM
Time Frame: The body temperature of the patient are recorded in the preoperative period.
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It is the form that includes the patient's body temperature.
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The body temperature of the patient are recorded in the preoperative period.
|
|
VITAL FINDINGS REGISTRATION FORM
Time Frame: The pulse of the patient are recorded in the preoperative period.
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It is the form that includes the patient's pulse.
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The pulse of the patient are recorded in the preoperative period.
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VITAL FINDINGS REGISTRATION FORM
Time Frame: The respiratory of the patient are recorded in the preoperative period.
|
It is the form that includes the patient's respiratory.
|
The respiratory of the patient are recorded in the preoperative period.
|
|
VITAL FINDINGS REGISTRATION FORM
Time Frame: The blood pressure of the patient are recorded in the preoperative period.
|
It is the form that includes the patient's blood pressure.
|
The blood pressure of the patient are recorded in the preoperative period.
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Muzeyyen Ataseven, Istanbul Marmara Universty
- Study Director: Nuray Sahin Orak, Istanbul Nisantasi University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pain
- Neurologic Manifestations
- Mental Disorders
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Anxiety Disorders
- Acute Pain
- Therapeutics
- Lipids
- Complementary Therapies
- Physical Therapy Modalities
- Food
- Diet, Food, and Nutrition
- Physiological Phenomena
- Food and Beverages
- Rehabilitation
- Plant Preparations
- Biological Products
- Complex Mixtures
- Plant Oils
- Oils
- Dietary Fats
- Fats
- Dietary Fats, Unsaturated
- Therapy, Soft Tissue
- Musculoskeletal Manipulations
- Fats, Unsaturated
- Massage
- Sesame Oil
Other Study ID Numbers
- mataseven
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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