- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04861753
The Effects of Reiki and Back Massage on the Pain and Vital Signs
April 24, 2021 updated by: HEDİYE UTLİ, Mardin Artuklu University
The Effects of Reiki and Back Massage on the Pain and Vital Signs of Women After Abdominal Hysterectomy: A Randomized Controlled Trial
The practice of Reiki and back massage applications in support of pharmacological treatment is among the nursing initiatives and these practices increase the autonomy of the profession.
The aim of this study was to determine the effects of Reiki and back massage on pain, analgesic use and vital signs in women who had undergone open abdominal hysterectomy.
This was an experimental study with a single, blinded, pretest-posttest control group.
The population of the study consisted of women who had abdominal hysterectomy in the Obstetrics Clinics at Gazi Yasargil Training and Research Hospital and Dicle University Hospital between July 2017 and February 2018.
The patients were divided into three groups: Reiki, back massage and control, with 34 patients in each group.
Reiki or back massage were applied for 20 minutes once a day to the patients in the Reiki and back massage groups.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study was carried out to determine the effect of Reiki and back massage application on pain, analgesic use and vital signs in women underwent open abdominal hysterectomy.
This study used an experimental pretest and posttest design with two experimental groups (Reiki and back massage), and a control group.
The population of the study consisted of women who underwent abdominal hysterectomy in the Obstetrics Clinics of the Gazi Training and Research Hospital and Dicle University Hospital between July 2017 and February 2018.
Open abdominal hysterectomy is usually performed in clinics on a planned basis.The data were collected by the researcher in the clinic by the face-to-face interview method using the Patient Information Form, the Numeric Pain Rating Scale (NPRS), and the Vital Signs and Postoperative Analgesic Follow-up Form.
Study Type
Observational
Enrollment (Actual)
102
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Mardin, Turkey, 47200
- Hediye Utli
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 61 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Probability Sample
Study Population
Open abdominal hysterectomy is usually performed in clinics on a planned basis.
Patients undergoing open abdominal hysterectomy are hospitalized over 1-2 days before the surgery and they are discharged on the postoperative 3 rd day if there is no postoperative complication.
Routine analgesics and antibiotics are given to all patients in the postoperative period.
Description
Inclusion Criteria:
- Patients who underwent surgery in elective conditions,
- were hospitalized for at least two days after surgery,
- did not develop any serious complications after surgery,
- were operated on under general anesthesia,
- had no previous Reiki or back massage,
- had a pain level of 3 or above according to the Numeric Pain Rating Scale,
- had no cognitive, affective or communication problems,
- used only one type of analgesic (a non-narcotic analgesic)
- did not use patient-controlled analgesics.
Exclusion Criteria:
- Patients with chronic disease (such as hypertension, cardiovascular disease),
- severe complications after surgery (such as bleeding, infection),
- those who were taking narcotic analgesics.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Reiki
The modern-day Reiki (pronounced "ray-kee") practiced in the United States originated in Japan with Mikao Usui in the early 1900s.
Reiki is a complementary and adjuvant therapeutic technique.
Reiki, which is classified as an "energy healing therapy", is a technique of channeling universal energy in order to reduce stress, promote relaxation, and enhance well-being.
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In the current study, at the beginning of the treatment, the researcher held his hands 2-3 cm above the patient sand adjusted the aura of the patient by making circular movements from the head to the feet.
After this process of aura attunement, the researcher placed his hands directly on the patient's body.
In the areas where the practitioner had placed his hands for an average of three minutes, starting from between the eyes, the researcher felt various degrees of warmth and tingling in his palms.
Only the back was left exposed to prevent the patient becoming cold.
The researcher took a little non-aromatic baby oil in hand and heated it, then began a 20-minute-long massage.
The massage consisted of 6.5 minutes of effleurage (stroking), 3.5 minutes of petrissage (kneading), 13 minutes of effleurage and seven minutes of petrissage.
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Back massage
Massage therapy involves the manipulation of the soft tissues of the body by touch.
It consists of gentle movements such as effleurage, petrissage and percussion.
|
In the current study, at the beginning of the treatment, the researcher held his hands 2-3 cm above the patient sand adjusted the aura of the patient by making circular movements from the head to the feet.
After this process of aura attunement, the researcher placed his hands directly on the patient's body.
In the areas where the practitioner had placed his hands for an average of three minutes, starting from between the eyes, the researcher felt various degrees of warmth and tingling in his palms.
Only the back was left exposed to prevent the patient becoming cold.
The researcher took a little non-aromatic baby oil in hand and heated it, then began a 20-minute-long massage.
The massage consisted of 6.5 minutes of effleurage (stroking), 3.5 minutes of petrissage (kneading), 13 minutes of effleurage and seven minutes of petrissage.
|
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Control
Routine postoperative care was given to the control group without any intervention
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Pain Rating Scale (NPRS)
Time Frame: 1st postoperative days
|
This scale gives pain a numeric score, from the absence of pain (0 integers) to unbearable pain (10 integers).
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1st postoperative days
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Vital Signs and Postoperative Analgesic Follow-up Form (VSPAFF)
Time Frame: 1st postoperative days
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This consists of questions about the application of reiki and back massage, information about the patients' vital signs, including pulse rate (min), respiratory rate (min), blood pressure (mmHg) at the time of measurement, as well as information about the number and doses (milligrams) of analgesics taken postoperatively.
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1st postoperative days
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Numeric Pain Rating Scale (NPRS)
Time Frame: 2 nd postoperative days
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This scale gives pain a numeric score, from the absence of pain (0 integers) to unbearable pain (10 integers).
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2 nd postoperative days
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Vital Signs and Postoperative Analgesic Follow-up Form (VSPAFF)
Time Frame: 2 nd postoperative days
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This consists of questions about the application of reiki and back massage, information about the patients' vital signs, including pulse rate (min), respiratory rate (min), blood pressure (mmHg) at the time of measurement, as well as information about the number and doses (milligrams) of analgesics taken postoperatively.
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2 nd postoperative days
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 9, 2017
Primary Completion (Actual)
February 9, 2018
Study Completion (Actual)
February 9, 2018
Study Registration Dates
First Submitted
April 5, 2021
First Submitted That Met QC Criteria
April 24, 2021
First Posted (Actual)
April 27, 2021
Study Record Updates
Last Update Posted (Actual)
April 27, 2021
Last Update Submitted That Met QC Criteria
April 24, 2021
Last Verified
April 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ArtukluU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
IPD Plan Description
After the article is accepted for publication, it will be shared with other researchers.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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