MedPath

Effectiveness of Oculus quest and Kinect azure in improving stress, burnout, performance, and quality of life among entrepreneurs

Not Applicable
Registration Number
CTRI/2022/05/042608
Lead Sponsor
KP Salve Institute of Medical Sciences and Research Centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.He can understand or fluently speak Hindi or English;

2.He is willing and able to give informed consent for participation in the trial.

Exclusion Criteria

1.Presence of physical disabilities, which make using the interventions difficult.

2.Self-reported severe psychological or medical disabilities, which make the interventions too confusing (including self-reported dementia).

3.Neurological conditions (eg, Parkinsonâ??s disease, epilepsy, stroke or dementias),

4.Significant visual, auditory or balance impairment;

5.Current receipt of another intensive psychological therapy (or about to start it within the 4-week trial therapy window);

6.Primary diagnosis of alcohol or substance disorder or personality disorder;

7.Unable to watch VR videos (eg, blindness).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Stressors of entrepreneurial employment <br/ ><br>2. Burnout measuring scale <br/ ><br>3. SF-12Timepoint: The questionnaires for evaluating entrepreneurship stress, burnout, quality of life, and performance will be provided at the start of the program and every last day of the training week for 4 weeks.
Secondary Outcome Measures
NameTimeMethod
Post-intervention questionnaireTimepoint: A postintervention questionnaire will be conducted after completion of the intervention period i.e. at the end of the 4th week to assess the participantâ??s perception of the VR platform and its components.;Pretraining and post-training questionnaireTimepoint: At baseline, the confidence level of each participant with the device will be assessed using a pretraining questionnaire. The participants will be given the training to use the device. After this, the post training questionnaire will be completed at baseline only.
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