Video-based Intervention to Reduce Anxiety in Patients Undergoing Elective PCI
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21+
SponsorTan Tock Seng Hospital
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
adults scheduled for elective percutaneous coronary intervention
voluntary participation
ability to understand english
age 21 and above
Disqualifiers
patients participating in other studies
outpatient PCI, urgent or emergency PCI
medically unstable
cognitive impairment
Trial design
Design model
Parallel
Treatments tested in this trial
Video intervention
BehavioralParticipants will watch a structured educational video explaining PCI
Treatment groups
144 Participants
are divided into 2 treatment groupsGroup A: Nurse-led video educationExperimental treatment 1 intervention
Group B: Standard of careNo intervention 0 interventions
Trial outcomes
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).
Time frame
Baseline (before intervention) After intervention / before PCI procedureSponsors and contacts
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Source ClinicalTrials.gov