Actively Recruiting
Effect of a Nurse-led Video-based Educational Intervention on Anxiety Among Hospitalised Patients Undergoing Elective Percutaneous Coronary Intervention: a Non-randomised Controlled Study
Led by Tan Tock Seng Hospital · Updated on 2026-03-24
144
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a video-based educational intervention to reduce anxiety in hospitalised patients who are scheduled for elective percutaneous coronary intervention (PCI). The study aims to compare anxiety levels between patients who watch a structured educational video about the PCI procedure and those who receive usual care without the video. Anxiety will be measured using the State-Trait Anxiety Inventory before and after the intervention to assess its impact. Participants are divided into two groups without randomisation. One group watches a nurse-led video explaining the PCI procedure and what to expect during hospitalisation. The other group receives the standard pre-procedural care provided by the hospital, without the video intervention. This approach helps evaluate whether the video reduces anxiety before the PCI. During the study, participants' anxiety levels will be assessed at baseline and after the intervention but before the PCI procedure. The study involves measuring anxiety changes to understand the video intervention's effect. Participation includes watching the video or receiving usual care, with assessments carried out in the hospital setting. The study is sponsored by Tan Tock Seng Hospital and plans to complete by June 2027.
CONDITIONS
Brief Title
Video-based Intervention to Reduce Anxiety in Patients Undergoing Elective PCI
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults scheduled for elective percutaneous coronary intervention
- Voluntary participation
- Ability to understand English
- Age 21 and above
You will not qualify if you...
- Patients participating in other studies
- Outpatient PCI, urgent or emergency PCI
- Medically unstable
- Cognitive impairment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Short period before the PCI procedure
Participants watch a structured educational video explaining the percutaneous coronary intervention procedure and expected experiences during hospitalisation.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Tan Tock Seng Hospital
Singapore, Singapore
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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