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New treatment option for Total Knee Arthroplasty (Postoperative Pain)
Official title REIKI IN TOTAL KNEE ARTHROPLASTY PATIENTS (REIKI TKA )
ClinicalTrials.gov ID: NCT07442435
What this study is testing
- What it's testing
- Total knee arthroplasty (TKA) is commonly performed to improve mobility and quality of life in patients with degenerative joint diseases. However, severe postoperative pain, limited mobilization, and fluctuations in vital signs negatively affect recovery, particularly within the first 72 hours after surgery.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Adults aged 18 years and older
- Undergoing elective (planned) primary total knee arthroplasty
- Not receiving general anesthesia
- Able to communicate effectively and understand the study protocol
- Hospitalized for two days following total knee arthroplasty
You likely can't join if
- Refusal to participate in the study
- Previous total knee arthroplasty or revision knee surgery
- Prior experience with Reiki, Therapeutic Touch, Healing Touch, or other energy-based therapies
- Development of serious postoperative complications (e.g., bleeding, infection)
- Diagnosis of chronic pain syndrome (e.g., fibromyalgia, chronic low back pain)
- Neuropsychiatric disorders such as dementia, Alzheimer's disease, schizophrenia, or major depressive disorder
See the full eligibility criteria
- Adults aged 18 years and older
- Undergoing elective (planned) primary total knee arthroplasty
- Not receiving general anesthesia
- Able to communicate effectively and understand the study protocol
- Hospitalized for two days following total knee arthroplasty
- Refusal to participate in the study
- Previous total knee arthroplasty or revision knee surgery
- Prior experience with Reiki, Therapeutic Touch, Healing Touch, or other energy-based therapies
- Development of serious postoperative complications (e.g., bleeding, infection)
- Diagnosis of chronic pain syndrome (e.g., fibromyalgia, chronic low back pain)
- Neuropsychiatric disorders such as dementia, Alzheimer's disease, schizophrenia, or major depressive disorder
- Current use of psychotropic medications
- Regular use of opioids or corticosteroids
- Use of patient-controlled analgesia (PCA)
- Major surgery or severe trauma within the past 6 months
- Admission to the intensive care unit postoperatively
The study team makes the final eligibility decision.
Where it's taking place
- Sinop, Turkey (Türkiye)
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Sinop, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.