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The Effect of Video-Assisted Discharge Education After Total Hip Replacement Surgery

NCT04774562 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 31

Last updated 2021-03-01

No results posted yet for this study

Summary

Abstract Objective: The aim of this study was to investigate the effect of a video-assisted discharge education program on activities of daily living, functionality, and patient satisfaction after total hip replacement (THR) surgery.

Methods: This study included 31 participants who were randomly divided in the physiotherapy (PT) group (n=18), and the video-assisted discharge education (VADE) group (n=13). Both groups received a physiotherapy program. VADE group was additionally received VADE program. In both groups, all education programs were given face to face. Data were collecting using visual analog scale (VAS), Harris Hip Score (HHS), Nottingham Extended Activities of Daily Living Scale (NEADL), Tampa Scale of Kinesiophobia (TSK) and Patient Satisfaction Questionnaire at 1st week and 3rd month.

Practice Implications: The current study has contributed to the development of video-assisted health technologies.

Conditions

  • Total Hip Replacement
  • Patient Education
  • Patient Satisfaction
  • Activities of Daily Living

Interventions

BEHAVIORAL

Video-Assisted Discharge Education (VADE)

Video-Assisted Discharge Education (VADE): Information about THR, preventive rehabilitation approaches, transfer activities, using stairs, self-care activities.

BEHAVIORAL

Physiotherapy (PT) Program

Physiotherapy (PT): Breathing exercises, positioning, hip range of motion and strengthening exercises, and information about walking and ambulation.

Sponsors & Collaborators

  • Pamukkale University

    collaborator OTHER

  • Akdeniz University

    collaborator OTHER

  • Ozum Cetinkaya Eren

    lead OTHER

Principal Investigators

  • Ozum Cetinkaya Eren, PT, MSc. · Alanya Alaaddin Keykubat University

  • Nihal Buker, Assoc.Prof. · Pamukkale University

  • Hasan Atacan Tonak, Asst.Prof. · Akdeniz University

  • Mustafa Urguden, Prof. Dr. · Akdeniz University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-04
Primary Completion
2019-01-01
Completion
2019-07-19

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 NCT04774562 on ClinicalTrials.gov