Effect of Video Education on Daily Life Quality and Wound Care in Total Hip Arthroplasty Patients

NCT ID: NCT06523829

Last Updated: 2024-07-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 70 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-02-03
• Study Completion Date: 2022-10-05

Brief Summary

This study was conducted to examine the effects of video-based education on the activities of daily living, wound healing and prosthesis dislocation of patients who had total hip replacement surgery.

The main questions it aims to answer are:

Total hip replacement patients who received video-based education had higher postoperative daily living activities scale mean scores than patients who did not receive education.

Total hip replacement patients who received video-based education had lower postoperative Oxford Hip Score scale mean scores than patients who did not receive education.

Total hip replacement patients who received video-based education had lower postoperative Patient and Observer Scar Assessment scale mean scores than patients who did not receive education.

Detailed Description

The study was conducted in Balikesir Bandırma Education and Research Hospital, Orthopedics Clinic. Patients who met the inclusion criteria were randomly assigned to the intervention (video-based education) and control (standard nursing care) groups using randomizer.org. In collecting the study data; Individual Identification Form, Standardized Mini Mental Test, Barthel Daily Living Activities Index, Oxford Hip Score, Patient and Observer Scar Assessment Scale were used. Individual Identification Form, Barthel Daily Living Activities Index and Oxford Hip Score were applied to both groups before surgery. The intervention group received video-based education before surgery, the control group did not receive any education and received routine nursing care. On the 5th day after surgery, both groups were applied Barthel Daily Living Activities and Patient and Observer Scar Assessment Scale. Video-based education was repeated on the 2nd or 3rd day after surgery to the intervention group, and the control group received routine nursing care. Before discharge, video-based education was uploaded to the phones or computers of the patients and caregivers in the intervention group, and patients and caregivers were able to benefit from this education video whenever they wanted. Patients in the control group were discharged after receiving routine discharge education. Barthel Daily Living Activities, Oxford Hip Score and Patient and Observer Scar Assessment Scale were applied to both groups on the 30th day after surgery. Descriptive statistical methods (frequency, mean) were applied in the analysis of the data. Student t test was used in the analysis of normally distributed variables in independent groups, and the relationship between multiple independent variables was evaluated with the ANOVA test. Variance analysis was used in repeated measurements in the evaluation of quantitative data within the group. Pearson correlation analysis was used in the evaluation of the relationship between quantitative variables, and Fisher's Exact and Pearson Chi-square tests were used in the comparison of qualitative data.

Conditions

Arthroplasty, Replacement, Hip

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: DOUBLE

Study Groups

Group given video-based training

The application of the study to the active group;

• In addition to routine nursing care in the ward, video and education booklet were used. Video education was given to the patient and caregiver individually in the patient room. Watching the video takes 12 minutes.
• Video-based education was given in the preoperative period, on the 2nd-3rd postoperative day and at the discharge stage.

Group Type: ACTIVE_COMPARATOR

GROUP GIVEN VIDEO TRAINING

Intervention Type: OTHER

Video-based training was given to this group.

GROUP RECEIVING ROUTINE NURSING CARE

The application of the study to the control group; The patient was informed about the process before and after the surgery by the physician and the nurse working in the ward that day. The patient's pre-operative, surgical preparation, post-operative and discharge periods were carried out by different nurses due to work schedules. The patients were prepared by the nurse working in the ward that day on the day of surgery and sent to the operating room. After the surgery, the patients were given patient care in the ward and their follow-up and treatments were performed. During the discharge period, discharge information was given and discharge procedures were carried out.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

GROUP GIVEN VIDEO TRAINING

Video-based training was given to this group.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patients who volunteered to participate in the study,
• Are conscious, oriented and cooperative,
• Are over 18 years of age,
• Speak Turkish,
• Are at least primary school graduates,
• Have received the Standardized Mini Mental Test and scored over 23 points according to the guideline were included.

Exclusion Criteria

• Patients with communication problems (hearing, visual impairment)
• Patients diagnosed with a psychiatric disease
• Patients whose mobilization was not permitted by the physician were not included.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Bandırma Onyedi Eylül University

OTHER

Sponsor Role: lead

Responsible Party

AYŞE SİNEM TAŞ

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

AYŞE SİNEM TAŞ, PHD

Role: PRINCIPAL_INVESTIGATOR

BANDIRMA ONYEDİ EYLÜL ÜNİVERSİTESİ

Locations

Bandirma Eğitim Ve Araştirma Hastanesi

Balıkesir, Balikesi̇r, Turkey (Türkiye)

Countries

Turkey (Türkiye)

References

Tas AS, Eser I. The Effect of Video-Based Education on Activities of Daily Living and Wound Healing of Patients with Total Hip Replacement: Randomised Controlled Trials. Nurs Rep. 2025 Oct 4;15(10):356. doi: 10.3390/nursrep15100356.

Reference Type: DERIVED

PMID: 41149671 (View on PubMed)

Other Identifiers

BandirmaOnyediEylulU-AST-01

Identifier Type: -

Identifier Source: org_study_id