NCT06523829

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 3, 2022

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 5, 2022

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 5, 2022

Completed
1.8 years until next milestone

First Submitted

Initial submission to the registry

July 23, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

July 26, 2024

Completed
Last Updated

July 26, 2024

Status Verified

July 1, 2024

Enrollment Period

7 months

First QC Date

July 23, 2024

Last Update Submit

July 25, 2024

Conditions

Keywords

Daily life activitiesWound HealReplacement, Hip

Outcome Measures

Primary Outcomes (1)

  • Number of patients whose daily living activities increased thanks to video training

    Barthel Daily Living Activities Index will be used to evaluate this result. Cronbach alpha value was calculated as 0.90. ADL is the most preferred evaluation index among similar indexes that evaluates the level of independence of individuals in their daily activities. Barthel Index evaluates 10 areas including nutrition, washing, dressing, self-care, bowel care, bladder care, toilet use, mobility, going up and down stairs and transferring from wheelchair to bed and the lowest score is 0 and the highest score is 100. 0-20 points indicate that the individual is fully dependent, 21-61 points indicate that the individual is highly dependent, 62-90 points indicate that the individual is moderately dependent, 91-99 points indicate that the individual is slightly dependent and 100 points indicate that the individual is fully independent. In this study, Cronbach alpha coefficient of "Barthel Daily Living Activities Index" was found as 0.859.

    Change measurements for each participant were made at baseline, day 5, and day 30 after surgery.

Secondary Outcomes (1)

  • Number of patients whose wound healing improved thanks to video training

    Change measurements for each participant were made on day 5 and day 30 after surgery.

Study Arms (2)

Group given video-based training

ACTIVE COMPARATOR

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.

Other: GROUP GIVEN VIDEO TRAINING

GROUP RECEIVING ROUTINE NURSING CARE

NO INTERVENTION

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.

Interventions

Video-based training was given to this group.

Group given video-based training

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bandirma Eğitim Ve Araştirma Hastanesi

Balıkesir, Balikesi̇r, 10200, Turkey (Türkiye)

Location

Related Publications (1)

  • 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.

Study Officials

  • AYŞE SİNEM TAŞ, PHD

    BANDIRMA ONYEDİ EYLÜL ÜNİVERSİTESİ

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, CARE PROVIDER
Masking Details
Participants were not informed of which group they were in when they agreed to participate in the study. Similarly, caregivers and hospital staff were not informed about the groups. Only the researcher knew which group the participants were in.
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: This study was conducted as a randomized controlled trial.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

July 23, 2024

First Posted

July 26, 2024

Study Start

February 3, 2022

Primary Completion

September 5, 2022

Study Completion

October 5, 2022

Last Updated

July 26, 2024

Record last verified: 2024-07

Data Sharing

IPD Sharing
Will not share

Locations