The Effect of Acupressure in Patients With Knee Osteoarthritis
The Effect of Acupressure on Pain, Functional Status and Quality of Life in Patients With Knee Osteoarthritis
1 other identifier
interventional
90
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable knee-osteoarthritis
Started Mar 2015
Shorter than P25 for not_applicable knee-osteoarthritis
1 active site
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
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 11, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
November 11, 2015
CompletedFirst Submitted
Initial submission to the registry
December 21, 2021
CompletedFirst Posted
Study publicly available on registry
February 14, 2022
CompletedAugust 17, 2022
August 1, 2022
3 months
December 21, 2021
August 15, 2022
Conditions
Keywords
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)
EXPERIMENTALThe 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.
Control group
NO INTERVENTIONThecontrol group was performed with 45 patients. Any application was not performed for the control group.
Interventions
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.
Eligibility Criteria
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
- TC Erciyes Universitylead
- Pınar TEKİNSOY KARTINcollaborator
- Rabiye ÇIRPANcollaborator
Study Sites (1)
Nigde Omer Halisdemir University
Niğde, Ni̇ğde, 51240, Turkey (Türkiye)
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.
PMID: 41055613DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Tuğba AYDEMİR, RN, MSc
Nigde Omer Halisdemir University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- 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