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Use of Video with Simulation to reduce Anxiety in a Patient Undergoing a Cardiac Procedure

Efficacy of a Simulated Video on the State anxiety score and cardiorespiratory parameters of patients undergoing Percutaneous Cardiac Procedure: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3g96g2v
Enrollment
Unknown
Registered
2024-08-22
Start date
2024-05-07
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Anxiety

Interventions

For the random allocation process of participants, a randomization scheme was used based on the random number generator in the Statistical Package for the Social Sciences software version 21.0 generat
J01.897.280

Sponsors

Programa de Pós-Graduação strictu sensu em Atenção à Saúde
Lead Sponsor
Universidade Federal do Triângulo Mineiro
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients undergoing coronary angiography with the possibility of conversion to ad hoc angioplasty and elective or emergency percutaneous transluminal coronary angioplasty aged 18 years or older; of both sexes

Exclusion criteria

Exclusion criteria: Patients who are using sedative or anxiolytic medications at the time of data collection will be excluded from the study; and who are unable to maintain dialogue with the researcher to answer the items in the data collection instrument

Design outcomes

Primary

MeasureTime frame
It is expected to find a reduction in anxiety levels among participants undergoing the intervention, verified using the Student t test for independent samples and intra group analysis with the t test for dependent groups, based on the observation of a reduction in state-anxiety scores on pre- and post-intervention measurements

Secondary

MeasureTime frame
It is expected to demonstrate the normality of the cardiorespiratory parameters among the participants submitted to the intervention, verified by means of the Student t Test for independent samples and the intra-group analysis with the t test for dependent groups, from the verification of the maintenance of normality of cardiorespiratory parameters in pre and post intervention measurements

Countries

Brazil

Contacts

Public ContactMaria Helena Barbosa

Programa de Pós-Graduação strictu sensu em Atenção à Saúde

mhelena331@hotmail.com+55(34)9 91669447

Outcome results

None listed

Source: REBEC (via WHO ICTRP)