Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04861753
Other study ID # ArtukluU
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 9, 2017
Est. completion date February 9, 2018

Study information

Verified date April 2021
Source Mardin Artuklu University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 102
Est. completion date February 9, 2018
Est. primary completion date February 9, 2018
Accepts healthy volunteers No
Gender Female
Age group 25 Years to 65 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Reiki and back massage
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.

Locations

Country Name City State
Turkey Hediye Utli Mardin

Sponsors (1)

Lead Sponsor Collaborator
Mardin Artuklu University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numeric Pain Rating Scale (NPRS) This scale gives pain a numeric score, from the absence of pain (0 integers) to unbearable pain (10 integers). 1st postoperative days
Primary Vital Signs and Postoperative Analgesic Follow-up Form (VSPAFF) 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. 1st postoperative days
Primary Numeric Pain Rating Scale (NPRS) This scale gives pain a numeric score, from the absence of pain (0 integers) to unbearable pain (10 integers). 2 nd postoperative days
Primary Vital Signs and Postoperative Analgesic Follow-up Form (VSPAFF) 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. 2 nd postoperative days
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05559255 - Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI N/A
Completed NCT04748367 - Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care N/A
Terminated NCT04356352 - Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain Phase 2/Phase 3
Completed NCT05057988 - Virtual Empowered Relief for Chronic Pain N/A
Completed NCT04466111 - Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
Recruiting NCT06206252 - Can Medical Cannabis Affect Opioid Use?
Completed NCT05868122 - A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy Phase 3
Active, not recruiting NCT05006976 - A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study N/A
Completed NCT03273114 - Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain N/A
Enrolling by invitation NCT06087432 - Is PNF Application Effective on Temporomandibular Dysfunction N/A
Completed NCT05508594 - Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001 Phase 2/Phase 3
Recruiting NCT03646955 - Partial Breast Versus no Irradiation for Women With Early Breast Cancer N/A
Active, not recruiting NCT03472300 - Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
Completed NCT03678168 - A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries N/A
Completed NCT03286543 - Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System N/A
Completed NCT03931772 - Online Automated Self-Hypnosis Program N/A
Completed NCT02913027 - Can We Improve the Comfort of Pelvic Exams? N/A
Terminated NCT02181387 - Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor? Phase 4
Recruiting NCT06032559 - Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment Phase 3
Active, not recruiting NCT03613155 - Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care