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Video Game Use in Hospitalized Individuals

Implementation of Immersive Virtual Reality in individuals hospitalized in service emergency hospital

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6y69tqv
Enrollment
Unknown
Registered
2021-11-09
Start date
2021-09-20
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

Hospitalization

Interventions

Crossover Clinical Trial that will be carried out in an emergency unit of a hospital in the interior of the state of São Paulo, which will evaluate a convenience sample of around 30 individuals, of bo
F04.754.137.506.662
N02.278.216.500.968.336

Sponsors

Universidade do Oeste Paulista
Lead Sponsor
Universidade do Oeste Paulista
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 43 years or over, of both genders, with heart failure, admitted to the emergency room and with a prescription for motor and respiratory physiotherapy will be included.

Exclusion criteria

Exclusion criteria: Patients with mean arterial pressure 120 millimeters of mercury (mmHg), heart rate 140 beats per minute (bpm), need for vasoactive medication, respiratory rate > 35 inspiration per minute (ipm) will be excluded from the study , acute clinical worsening, sleepy, uncooperative or unable to follow commands, individuals in contact precaution and in orotracheal intubation.

Design outcomes

Primary

MeasureTime frame
The following hemodynamic parameters will be evaluated before and after (1st, 3rd, 5th and 10th minute) both interventions: Heart rate will be determined by Polar heart rate monitor model S810i (Polar Electro, Finland). Systolic and diastolic blood pressure will be checked by Premium® sphygmomanometer (Wenzhou, Zhejiang China) and Littiman® stethoscope (class III model, St. Paul, Minnesota, USA), according to the VII Brazilian Guidelines on Hypertension. Partial oxygen saturation will be analyzed using a Quanta OX-201 digital finger oximeter. The double product will be obtained by multiplying the heart rate (measured in bpm) by the systolic blood pressure (measured in mmHg).

Secondary

MeasureTime frame
Will be evaluated before and after both interventions the mood and levels of anxiety and depression. Mood state will be assessed using the Brunel Mood Scale (BRUMS), validated in Brazil by Rohlfs and designed to provide rapid measurement of mood for cardiovascular rehabilitation programs to detect overtraining syndrome. This instrument comprises 24 mood indicators, divided into six subscales: anger, confusion, depression, fatigue, tension and vigor, and the sum of each subscale results in a score that can range from 0 to 16. The patient responds as experience such sensations through a 5-point scale (from 0=nothing and 4=extremely). The condition is set in the question “How do you feel now”, although other ways: “How have you been feeling for the last week, including today” or “How do you normally feel” can be used. The levels of anxiety and depression will be assessed using the Hospital Anxiety and Depression Scale (HADS), translated and validated by Botega, Bio, Zomignani, Garcia Jr. and Pereira (1995). It has 14 items with 7 for anxiety (HADS-A) and 7 for depression (HADS-D), with each item scoring from 0 to 3 for a total of 21 points for the scale. The cutoff value for each scale is = 9.

Countries

Brazil

Contacts

Public ContactClynton Correa
clyntoncorrea@medicina.ufrj.br+5521995226017

Outcome results

None listed

Source: REBEC (via WHO ICTRP)