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Preoperative Video-Based Education in Total Hip Arthroplasty

NCT07279974 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 96

Last updated 2025-12-12

No results posted yet for this study

Summary

This single-center, prospective, randomized controlled trial aims to evaluate the effect of preoperative video-based mobilization education on postoperative fear of movement (kinesiophobia), pain during first mobilization, and early mobilization characteristics in patients undergoing total hip arthroplasty. Ninety-six participants were randomized to receive either routine verbal education plus video-based education or routine verbal education alone. Postoperative outcomes were assessed using the Tampa Scale of Kinesiophobia (TSK), Numerical Pain Rating Scale (NPRS), and standardized mobilization observation forms.

Conditions

  • Total Hip Arthroplasty (THA)
  • Kinesiophobia
  • Postoperative Pain
  • Early Mobilization
  • Hip Osteoarthritis
  • Musculoskeletal Rehabilitation

Interventions

BEHAVIORAL

Video-Based Mobilization Education

A structured preoperative video-based mobilization training including demonstrations of bed exercises, mobilization with assistive devices, chair transfer, toilet use, stair negotiation, and postoperative precautions.

BEHAVIORAL

Standard Verbal Education

Routine preoperative verbal instruction provided by ward nurses.

Sponsors & Collaborators

  • Acibadem University

    lead OTHER

Principal Investigators

  • Nermin Ocaktan · Acıbadem Mehmet Ali Aydınlar University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-15
Primary Completion
2024-07-30
Completion
2024-07-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07279974 on ClinicalTrials.gov