Early Mobilization and Postoperative Complications in Hip Arthroplast

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorCyprus Aydin University

About this trial

Orthopedic surgical procedures, particularly total hip replacement, are of great importance in the older population in terms of regaining functional independence, reducing pain, and improving quality of life. In addition to surgical success, the postoperative recovery process, rehabilitation programs, patient education, and nursing care directly affect patients' clinical and functional outcomes.

Failure to implement early mobilization may negatively affect patients' recovery and increase the risk of complications. Delayed mobilization may prolong hospital stays and increase healthcare costs. The most common complications include deep vein thrombosis, pulmonary embolism, respiratory complications, muscle weakness, and joint stiffness. Delayed mobilization may also increase postoperative pain and functional limitations, thereby restricting patients' ability to perform independent activities of daily living.

Patient education during the postoperative period is one of the key factors supporting the success of early mobilization. Education provided to patients regarding postoperative positioning, breathing exercises, pain management, protection of the prosthetic area, and the importance of mobilization can help reduce complications and improve patient adherence. When education is planned individually under the guidance of nurses, it supports functional independence and facilitates the rehabilitation process.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Inclusion Criteria Having undergone arthroplasty surgery at Dr. Burhan Nalbantoğlu State Hospital in Nicosia, TRNC.

Disqualifiers

Not having undergone arthroplasty surgery at Dr. Burhan Nalbantoğlu State Hospital in Nicosia, TRNC.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Early Mobilization Education

    Behavioral

    Participants in the intervention group will receive early mobilization education based on the Arthroplasty Patient Education Booklet. The education will be provided by the nurse/intervention provider and will include information on the importance of early mobilization, postoperative mobilization practices, and measures to prevent postoperative complications. The intervention will be provided in addition to routine postoperative care. Participants will be followed during the postoperative period to evaluate the effects of early mobilization education on postoperative complications.

  • Routine Postoperative Care

    Other intervention

    Participants will receive routine postoperative care provided by the clinical team according to standard clinical practice.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Intervention GroupExperimental treatment 2 interventions
Group B: Control GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Number of Participants With Postoperative Complications

Postoperative complications following hip arthroplasty will be assessed and recorded, and the number of participants experiencing one or more postoperative complications will be compared between the intervention and control groups.

Time frame
Up to 1 month after surgery

Secondary outcomes

1

Hip Function Assessed Using the Harris Hip Score

Hip function will be assessed using the Harris Hip Score (HHS) and compared between the intervention and control groups. The Harris Hip Score ranges from 0 to 100, with higher scores indicating better hip function.

Time frame
Up to 1 month after surgery

Other outcomes

Sponsors and contacts

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