NCT03553901

Brief Summary

Acupressure is an ancient manual therapy which fingers are used to press key points on the body. These points are the same with acupuncture points but in contrast to acupuncture, acupressure uses gentle but firm pressure with fingers and hands. The purpose of this study is to investigate effect of acupressure onto GB30 poin for ventrogluteal intramuscular injection pain.The study was designed as a prospective, single-blind, crossover study. The study included 72 volunteer students attending Faculty of Health Sciences, Nursing Department.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2016

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2016

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2017

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2017

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

May 30, 2018

Completed
13 days until next milestone

First Posted

Study publicly available on registry

June 12, 2018

Completed
Last Updated

June 13, 2018

Status Verified

June 1, 2018

Enrollment Period

9 months

First QC Date

May 30, 2018

Last Update Submit

June 11, 2018

Conditions

Outcome Measures

Primary Outcomes (1)

  • Assessment of pain during intramuscular injection with 10 cm VAS (Visual Analog Scale)

    Assessment of pain during intramuscular injection will be marked on 10 cm VAS scale 0-10 ( 0:no pain 10:Worst possible pain ) by the patient and will be measured

    2 minutes

Study Arms (2)

Acupressure

EXPERIMENTAL

Acupressure is applied before injection

Procedure: Acupressure

Control group

NO INTERVENTION

acupressure is not applied before injection

Interventions

AcupressurePROCEDURE

Acupressure was performed before the injection onto GB30 point

Acupressure

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Body Mass Index (BMI) of 18.5 to 29.9kg/m2
  • Voluntariness

You may not qualify if:

  • history of IM injection within 2 weeks

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (3)

  • Suhrabi Z, Taghinejad H. Effect of acupressure (UB32) on pain intensity in intramuscular injections. Iran J Nurs Midwifery Res. 2014 Jan;19(1):24-7.

    PMID: 24554956BACKGROUND
  • Hosseinabadi R, Biranvand S, Pournia Y, Anbari K. The Effect of Acupressure on Pain and Anxiety Caused by Venipuncture. J Infus Nurs. 2015 Nov-Dec;38(6):397-405. doi: 10.1097/NAN.0000000000000065.

    PMID: 26536327BACKGROUND
  • Chung JW, Ng WM, Wong TK. An experimental study on the use of manual pressure to reduce pain in intramuscular injections. J Clin Nurs. 2002 Jul;11(4):457-61. doi: 10.1046/j.1365-2702.2002.00645.x.

    PMID: 12100641BACKGROUND

MeSH Terms

Conditions

Acute Pain

Interventions

Acupressure

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Therapy, Soft TissueMusculoskeletal ManipulationsComplementary TherapiesTherapeuticsPhysical Therapy ModalitiesRehabilitation

Study Officials

  • Gökhan inangil

    Sultan Abdulhamid Han

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 30, 2018

First Posted

June 12, 2018

Study Start

September 1, 2016

Primary Completion

June 1, 2017

Study Completion

August 1, 2017

Last Updated

June 13, 2018

Record last verified: 2018-06