Video-based Intervention to Reduce Anxiety in Patients Undergoing Elective PCI
Effect of a Nurse-led Video-based Educational Intervention on Anxiety Among Hospitalised Patients Undergoing Elective Percutaneous Coronary Intervention: a Non-randomised Controlled Study
1 other identifier
interventional
144
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2026
1 active site
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
First Submitted
Initial submission to the registry
March 16, 2026
CompletedStudy Start
First participant enrolled
March 16, 2026
CompletedFirst Posted
Study publicly available on registry
March 20, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2027
March 24, 2026
March 1, 2026
1.2 years
March 16, 2026
March 19, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Anxiety level
Anxiety will be measured using the State-trait anxiety inventory (STAI), a validated self-report instrument assessing anxiety levels. Generally, higher scores indicate greater anxiety. Scores are often grouped: 20-37 (Low anxiety), 38-44 (Moderate anxiety), and 45-80 (High anxiety).
Baseline (before intervention) After intervention / before PCI procedure
Study Arms (2)
Nurse-led video education
EXPERIMENTALParticipants will watch a structured educational video explaining the percutaneous coronary intervention procedure, expected experiences during hospitalisation.
Standard of care
NO INTERVENTIONParticipants will receive routine pre-procedural care provided by the hospital without the video intervention.
Interventions
Participants will watch a structured educational video explaining PCI
Eligibility Criteria
You may qualify if:
- adults scheduled for elective percutaneous coronary intervention
- voluntary participation
- ability to understand english
- age 21 and above
You may not qualify if:
- patients participating in other studies
- outpatient PCI, urgent or emergency PCI
- medically unstable
- cognitive impairment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Tan Tock Seng Hospital
Singapore, Singapore
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Registered Nurse
Study Record Dates
First Submitted
March 16, 2026
First Posted
March 20, 2026
Study Start
March 16, 2026
Primary Completion (Estimated)
June 1, 2027
Study Completion (Estimated)
June 1, 2027
Last Updated
March 24, 2026
Record last verified: 2026-03