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Recruiting NCT07485088

NCT07485088 Video-based Intervention to Reduce Anxiety in Patients Undergoing Elective PCI

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Clinical Trial Summary
NCT ID NCT07485088
Status Recruiting
Phase
Sponsor Tan Tock Seng Hospital
Condition Procedural Anxiety
Study Type INTERVENTIONAL
Enrollment 144 participants
Start Date 2026-03-16
Primary Completion 2027-06

Eligibility & Interventions

Sex All sexes
Min Age 21 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Video intervention

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 144 participants in total. It began in 2026-03-16 with a primary completion date of 2027-06.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

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.

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

Frequently Asked Questions

Who can join the NCT07485088 clinical trial?

This trial is open to participants of all sexes, aged 21 Years or older, studying Procedural Anxiety. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07485088 currently recruiting?

Yes, NCT07485088 is actively recruiting participants. Visit ClinicalTrials.gov or contact Tan Tock Seng Hospital to inquire about joining.

Where is the NCT07485088 trial being conducted?

This trial is being conducted at Singapore, Singapore.

Who is sponsoring the NCT07485088 clinical trial?

NCT07485088 is sponsored by Tan Tock Seng Hospital. The trial plans to enroll 144 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology