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Impact of Multimedia Education Before Cerebral Angiography on Anxiety and Vital Signs in Patients

Effect of multimedia based pre procedural education on physiological and psychological parameters of patient undergone cerebral angiography: A randomized controlled clinical trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090831
Enrollment
60
Registered
2025-07-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: Z049- Encounter for examination and observation for unspecified reason

Interventions

Intervention1: The Multimedia Based Educational Intervention: The multimedia based educational intervention to teach patients about cerebral angiography which consisted of four main sections: explaini

Sponsors

Department of Radiodiagnosis and Imaging
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Individuals aged 19 to 60 years. 2.Being first time elective diagnostic cerebral femoral and radial catheterization recipients. 3.Having a sheath size of 5/6 french. 4.Free from certain medical conditions such as diabetes associated sensory issues or psychiatric diseases. 5.No visual or hearing impairments.

Exclusion criteria

Exclusion criteria: 1.Recent anticoagulant use, 2.Compromised skin integrity at the access site, 3.History of bleeding disorders. 4.Disoriented and loss of consciousness 5.Having vascular closure device

Design outcomes

Primary

MeasureTime frame
Reduction in anxiety levels as measured by The State-Trait Anxiety Inventory (STAI)Timepoint: 1 hr

Secondary

MeasureTime frame
1)Stabilization of vital signs such as blood pressure, heart rate, respiratory rate and Spo2 2)Reduction in discomfort as measured by the Discomfort scale 3)Reduction in pain as measured by the Numerical rating scale pain scores 4)Reduced incident of hematoma as measured by hematoma scale Timepoint: 1)1hr 2)For hematoma after 8 hrs

Countries

India

Contacts

Public ContactDr Manju Dhandapani

POST GRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH INSTITUTE,CHANDIGARH

ajay2509@gmail.com9914209385

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026