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The Effects of Acupressure on Pain, Swelling and Comfort in Patients With Femoral Fracture Surgery

The Effects of Acupressure on Pain, Swelling and Comfort in Patients With Femoral Fracture Surgery

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06914323
Enrollment
140
Registered
2025-04-06
Start date
2025-02-18
Completion date
2026-02-18
Last updated
2025-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acupressure

Brief summary

Pain is a subjective and unpleasant sensory and emotional experience associated with actual or potential tissue damage. Fractures result from a disruption in the continuity of bone, where bones are subjected to traction, twisting, or compression, causing damage to the surrounding muscular tissues. The treatment of displaced or complex fractures typically requires internal fixation surgery. 89% of fracture patients experience postoperative pain and swelling by the second day following open reduction and internal fixation surgery. These negative sensations can lead to increased pain, limb deformity, and neurovascular compression injuries. If postoperative pain is not adequately managed, it can affect wound healing, increase metabolism and oxygen consumption, and place additional strain on cardiopulmonary function. It is necessary to integrate alternative, non-pharmacological, non-invasive pain relief measures. Effectively and safely alleviating acute postoperative pain can enhance comfort, promote early mobilization, improve adherence to postoperative physical therapy, enhance quality of life and shorten hospital stays.

Interventions

PROCEDUREAcupressure

improvements in pain, limb swelling, and comfort

Sponsors

Hungkuang University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. The patient was hospitalized due to injuries from an accident, diagnosed with unilateral femoral fracture and underwent open reduction internal fixation surgery, hemiarthroplasty, and total hip arthroplasty. 2. Adults aged 18 years or older. 3. Conscious and able to communicate in Mandarin or Taiwanese (Min Nan). 4. Intact and without missing lower limbs. 5. Willing to sign the informed consent form after being briefed on the study objectives and procedures.

Exclusion criteria

1. Diagnosis of musculoskeletal tumors. 2. History of cerebrovascular accident or peripheral vascular neuropathy. 3. Major medical conditions such as cirrhosis, renal failure, heart failure, cancer, and severe brain diseases. 4. Edema caused by nutritional deficiency or mucinous causes. 5. Pregnant or lactating women. 6. Patients using patient-controlled analgesia post-surgery. 7. Severe psychiatric disorders or perceptual disorders. 8. Platelet count less than 20 x 10\^3/uL before screening. 9. Albumin less than 3.5g/dL before screening. 10. Individuals closely related to the trial personnel, such as immediate family or dependents of the principal investigator.

Design outcomes

Primary

MeasureTime frameDescription
Changes in painpost op day 1 to post op day 2Pain is measured using the Visual Analog Scale (VAS). The left end is labeled as no pain, which represents 0, and the right end as the most severe pain imaginable, which represents 100.
Change in limb swellingpost op day 1 to post op day 2Foot circumference at the midpoint of the line connecting the fifth toe to the lateral malleola is measured in centimeters for swelling assessment. A measuring tape is used. During the measurement, the patient is positioned in a supine posture.
Changes in patient comfortpost op day 1 to post op day 2Shortened General Comfort Questionnaire (SGCQ) for measuring comfort. The questionnaire consists of 28 items, assessed on a 6-point Likert scale ranging from strongly disagree to strongly agree. A score of 1 represents strongly disagree, while a score of 6 represents strongly agree. The total score ranges from 28 to 148, with higher scores indicating greater levels of comfort.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026