Anti-Stress Intervention Among Physicians Study (ASIP)

Charité University Medicine Berlin

Status: Completed

Conditions: Burnout, Psychological; Occupational Stress; Subjective Stress; Stress, Psychological

Treatments: Behavioral: Box Breathing; Behavioral: Everyday life control; Behavioral: Breathing and Mindfulness Exercise

Study type: Interventional

Funder types: Other

Identifiers

NCT06368791

30001479

Details and patient eligibility

About

Medical practice often comes with high stress. Stress negatively affects our health and well-being and is linked to doctors making mistakes, some of which can be deadly.

In this study, the effect of two quick stress-relief methods on daily stress levels is estimated. The two anti-stress exercises are designed to easily fit into daily routines:

1. Box breathing (6 minutes) is known to reduce stress and lower the heart rate. It is used by the military and law enforcement, among others, to manage stress.
2. Breathing and mindfulness exercise (10 minutes): This guided breathing and mindfulness intervention combines mindful breathing with simple body movements, developed to reduce the perceived level of stress.

The effectiveness of these interventions is being examined in a series of N-of-1 trials. Each participant can choose between the interventions. After being randomly allocated to an individual sequence of one-week intervention and control phases, the study begins. Participants record their stress levels daily over the four-week study period. The intervention is only performed in the intervention phases. Upon completing the study, the stress levels during the intervention phases are compared to those in the control phases. Each participant will receive an individual analysis based on the collected data. In addition, the investigators will estimate the effects at the population level.

Three months after the study, a survey will be sent to the participants to check if the benefits have persisted.

Enrollment: 145 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

• Physicians in training in Germany
• Weekly working time in medical activity of at least 9 hours
• Regular access to a mobile phone on which the "StudyU"-App can be installed
• Informed consent

Exclusion criteria

• Age <18 years
• Specialist training already completed
• No clinical activity during the study period or part of the study period (e.g. vacation, research activity, etc.)
• Participation in another intervention study during the study period
• Does not speak German
• Does yoga more than 4 times a month
• Meditates or performs breathing exercises on average more than 4 days per month
• Confirmed or suspected pregnancy
• Presence of a psychiatric disorder
• Presence of cardiovascular disease
• Presence of respiratory or pulmonary disease
• Presence of a neurological disease
• Substance abuse (for example, alcohol, drugs, or other)
• Planned surgery within the next 6 months
• Doctor's recommendation (or self-assessment) not to perform mindfulness or breathing exercises
• Lack of informed consent
• Employee of the Charité - Universitätsmedizin Berlin (due to data protection reasons, employees of the Charité - Universitätsmedizin Berlin will not be included in this study)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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145 participants in 2 patient groups

Box Breathing

Experimental group

Description:

In the intervention phase of the N-of-1 trial participants are instructed to perform box breathing intervention. During the control phase of the N-of-1 trial, participants are instructed to proceed with their daily activities as usual without engaging in the anti-stress intervention.

Treatment:

Behavioral: Everyday life control

Behavioral: Box Breathing

Breathing and Mindfulness Exercise

Experimental group

Description:

In the intervention phase of the N-of-1 trial participants are instructed to perform the guided breathing and mindfulness exercise. During the control phase of the N-of-1 trial, participants are instructed to proceed with their daily activities as usual without engaging in the anti-stress intervention.

Treatment:

Behavioral: Everyday life control

Behavioral: Breathing and Mindfulness Exercise