NCT05238350

Brief Summary

Abstract Pain is the most common symptom of osteoarthritis and affects people's functional status with quality of life. This study was conducted to determine the effect of acupressure on pain, functional status, and quality of life in patients living with knee osteoarthritis. Acupressure application and follow-ups were performed by the researcher in the patient's home environment. The study was performed with 90 patients, 45 in the intervention group and 45 in the control group. Acupressure was performed two days a week for four weeks with a total of eight sessions on the ST34, ST35, ST36, SP9, SP10, GB34 acupuncture points following an acupressure practice guide prepared by the researcher. It was determined that while the Visual Analog Scale (VAS), the Western Ontario and McMaster University Osteoarthritis Index (WOMAC) scores of the intervention group were higher than those of the control group before application, they had decreased after application. It was found that all subscale mean scores of the Short-Form Health Survey (SF-36) quality of life questionnaire increased after application in the intervention group. It was concluded that acupressure has decreased pain severity and increased the functional status and quality of life of patients with knee osteoarthritis. Keywords: Osteoarthritis, pain, nursing, acupressure.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable knee-osteoarthritis

Timeline
Completed

Started Mar 2015

Shorter than P25 for not_applicable knee-osteoarthritis

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 7, 2015

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 11, 2015

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 11, 2015

Completed
6.1 years until next milestone

First Submitted

Initial submission to the registry

December 21, 2021

Completed
2 months until next milestone

First Posted

Study publicly available on registry

February 14, 2022

Completed
Last Updated

August 17, 2022

Status Verified

August 1, 2022

Enrollment Period

3 months

First QC Date

December 21, 2021

Last Update Submit

August 15, 2022

Conditions

Keywords

OsteoarthritisPainNursingAcupressure.

Outcome Measures

Primary Outcomes (1)

  • Pain level in visual analogue scale (VAS)

    Pain severity scores were determined by measuring values that were chosen on VAS by patients. The numerical scale ranges from 0 "No pain", to 10 "Worst pain imaginable", and a numerical value is given to every 1 cm range to measure pain severity.

    baseline, change from baseline at 4th week;

Secondary Outcomes (2)

  • The Western Ontario and McMaster University Osteoarthritis Index (WOMAC) Osteoarthritis Index

    baseline, change from baseline at 4th week;

  • 36-Item Short-Form Health Survey (SF-36)

    baseline, change from baseline at 4th week;

Study Arms (2)

Acupressure (intervention group)

EXPERIMENTAL

The intervention group was performed with 45 patients. Acupressure was performed two days a week for four weeks with a total of eight sessions on the ST34, ST35, ST36, SP9, SP10, GB34 acupuncture points following an acupressure practice guide prepared by the researcher.

Procedure: Acupressure

Control group

NO INTERVENTION

Thecontrol group was performed with 45 patients. Any application was not performed for the control group.

Interventions

AcupressurePROCEDURE

Acupressure was performed two days a week for four weeks with a total of eight sessions on the ST34, ST35, ST36, SP9, SP10, GB34 acupuncture points following an acupressure practice guide prepared by the researcher.

Also known as: Control
Acupressure (intervention group)

Eligibility Criteria

Age38 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • years old and over
  • Diagnosed by a doctor with knee OA according to American College of Rheumatology (ACR) criteria
  • had three points and over on the VAS pain scale,
  • had no communication problems
  • did not have any significant knee trauma within the last six months or an intra-articular steroid injection
  • did not have any infection in the lower extremities or wounds, surgery or physiotherapy within the last six months
  • those who accepted to participate to the study.

You may not qualify if:

  • the patient is not willing to go on the study in any stage of the study and case of any adverse effect of acupressure.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nigde Omer Halisdemir University

Niğde, Ni̇ğde, 51240, Turkey (Türkiye)

Location

Related Publications (1)

  • Aydemir T, Cirpan R, Tekinsoy Kartin P. Impact of Acupressure on Pain, Functional Status, and Quality of Life in Individuals With Knee Osteoarthritis. J Manipulative Physiol Ther. 2025 Jan-Jun;48(1-5):204-213. doi: 10.1016/j.jmpt.2025.09.001. Epub 2025 Oct 7.

MeSH Terms

Conditions

Osteoarthritis, KneeOsteoarthritisPain

Interventions

Acupressure

Condition Hierarchy (Ancestors)

ArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Therapy, Soft TissueMusculoskeletal ManipulationsComplementary TherapiesTherapeuticsPhysical Therapy ModalitiesRehabilitation

Study Officials

  • Tuğba AYDEMİR, RN, MSc

    Nigde Omer Halisdemir University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: The study was conducted as an experimental study with a pre-posttest and a control group.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

December 21, 2021

First Posted

February 14, 2022

Study Start

March 7, 2015

Primary Completion

June 11, 2015

Study Completion

November 11, 2015

Last Updated

August 17, 2022

Record last verified: 2022-08

Locations