Video-based Intervention to Reduce Anxiety in Patients Undergoing Elective PCI
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Video intervention.
- Who it may be relevant to
- Registry conditions: Procedural Anxiety, Coronary Artery Disease, Percutaneous Coronary Intervention Patients. Basic parameters: from 21 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Singapore
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Effect of a Nurse-led Video-based Educational Intervention on Anxiety Among Hospitalised Patients Undergoing Elective Percutaneous Coronary Intervention: a Non-randomised Controlled Study
Overview
This study aims to evaluate the effectiveness of a video-based educational intervention in reducing anxiety among hospitalised patients scheduled for elective percutaneous coronary intervention (PCI). Participants will be assigned to either a video intervention group or a control group without randomisation. The intervention group will receive a structured educational video related to the PCI procedure, while the control group will receive usual care. Anxiety levels will be measured using the State-Trait Anxiety Inventory at baseline and after the intervention to determine whether the video intervention reduces anxiety before the procedure.
Interventions
- Behavioral Video intervention
Participants will watch a structured educational video explaining PCI
Primary outcome measures
- Anxiety level [Time frame: Baseline (before intervention) After intervention / before PCI procedure]
Eligibility criteria
Inclusion criteria
- adults scheduled for elective percutaneous coronary intervention
- voluntary participation
- ability to understand english
- age 21 and above
Exclusion criteria
- patients participating in other studies
- outpatient PCI, urgent or emergency PCI
- medically unstable
- cognitive impairment
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Non-randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
Singapore · 1 center
- Tan Tock Seng Hospital — Singapore
Identifiers
NCT: NCT07485088 · Project VIRA