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Horse-assisted Intervention, Heart Rate Variability & Stress

M

Medical University of Graz

Status

Begins enrollment in 2 months

Conditions

Psychological Stress

Treatments

Behavioral: watching the countryside
Behavioral: animal-assisted intervention

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

In this study, the effects of an animal-assisted intervention on people with increased stress levels are investigated. The data collected will be compared with those of participants with high stress levels but without animal-assisted intervention (participants only observe nature) and with a control group consisting of people without stress exposure.

The study will be performed in the following setting: Questionnaire examination on chronic stress, questionnaire on current well-being and heart rate variability (HRV) measurement before the horse-assisted intervention, one HRV measurement and one questionnaire examination (POMS) on current well-being after the horse-assisted intervention, one questionnaire (POMS) on current well-being 5 days after the horse-assisted intervention.

Full description

The early recognition of chronic stressors, which are often neglected by those affected until physical symptoms appear, is of essential importance. In addition to psychopharmacological therapy modalities, complementary methods such as animal-assisted intervention should also be considered in order to expand the therapeutic spectrum and thus prevent stress-associated consequential harms as early as possible.

Stress has gained importance in recent years not only in the medical context, but also due to its economic relevance. Chronic stress in particular leads to numerous medically relevant secondary diseases and to increased sick leaves and even permanent incapacity to work. One possible intervention to reduce stress could be animal-assisted intervention.

Primary hypothesis: The use of animal-assisted intervention in people diagnosed with chronic stressful situations will lead to measurable increases in heart rate variability.

Secondary hypothesis: The use of animal-assisted intervention in people diagnosed with chronic stressful situations leads to improved well-being (target parameter: POMS questionnaire)

Enrollment

123 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male, female and diverse
  • Age between 18-75 years

Exclusion criteria

  • Animal hair allergies (especially horse hair allergies, fear of horses)
  • Acute severe psychiatric conditions (e.g. psychosis)
  • Persons, unable to give signed informed consent,
  • All persons, who have not signed the informed consent form.

Trial design

Primary purpose

Prevention

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

Single Blind

123 participants in 3 patient groups

subjects with stress burden and animal-assisted intervention
Experimental group
Description:
The 20-minute horse-assisted intervention takes place in compliance with basic safety precautions (safety bar between horse and participant) and after safety instruction in handling the therapy horse. The horse can be touched or stroked more or less intensively, depending on the needs and current state of mind of the study participant.
Treatment:
Behavioral: animal-assisted intervention
subjects with stress burden and without animal-assisted intervention
Active Comparator group
Description:
Study participants only observe the natural environment.
Treatment:
Behavioral: watching the countryside
subjects without stress burden and with animal-assisted intervention
Active Comparator group
Description:
The 20-minute horse-assisted intervention takes place in compliance with basic safety precautions (safety bar between horse and participant) and after safety instruction in handling the therapy horse. The horse can be touched or stroked more or less intensively, depending on the needs and current state of mind of the study participant.
Treatment:
Behavioral: animal-assisted intervention

Trial contacts and locations

1

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Central trial contact

Bettina Frühwirth; Andreas Baranyi, M.D.

Data sourced from clinicaltrials.gov

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