Horse-assisted Intervention, Heart Rate Variability & Stress

Status Not yet recruiting

Clinical Trial Summary

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.

Clinical Trial 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) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05703165
Study type	Interventional
Source	Medical University of Graz
Contact	Andreas Baranyi, M.D.
Phone	004331638586241
Email	an.baranyi@medunigraz.at
Status	Not yet recruiting
Phase	N/A
Start date	March 1, 2023
Completion date	March 1, 2025

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT04680611` - Severe Asthma, MepolizumaB and Affect: SAMBA Study
Completed	`NCT05703087` - Positive Cueing in Knee Arthroplasty.	N/A
Completed	`NCT02541240` - Effects of an Intervention to Enhance Resilience in Physical Therapy Students	N/A
Completed	`NCT02629016` - Stress Reduction: A Pilot Study With Adolescents	N/A
Completed	`NCT01406028` - Does Emotional Support Decrease In Vitro Fertilization Stress?	N/A
Completed	`NCT00121160` - Health SMART (Stress Management and Relaxation Training) to Improve Vaccine Immune Response	Phase 1
Completed	`NCT02621775` - Effectiveness of Two Stress Management Programs in Adaptation Disorder With Anxiety (ADA)	N/A
Recruiting	`NCT04474418` - Psychometric Characterization of Patients With Cardiac Arrhythmias
Completed	`NCT03310112` - Mindfulness Training in U.S. Army Cohorts	N/A
Terminated	`NCT03893617` - Brief Stresses Experimental Study	Phase 1
Active, not recruiting	`NCT05542498` - Promoting Stress Management and Engagement in Introductory Physics Courses With Mindfulness and Relaxation	N/A
Completed	`NCT02394899` - Improving Parental Psychosocial Functioning and Early Developmental Outcomes in Children With Sickle Cell Disease	N/A
Terminated	`NCT00962273` - The Pandemic Stress Vaccine: A Resource to Enhance the Resilience of Healthcare Workers Facing an Infectious Outbreak	N/A
Completed	`NCT00451126` - Moderating Impact of Various Emotion Personality Factors on Salivary Cortisol Response to a TSST	N/A
Recruiting	`NCT06051500` - Psychological and Physiological Effects of Different Objects of Breath Meditation	N/A
Completed	`NCT02801045` - Art Therapy in Palliative Care: Study of Identification and Understanding of the Mechanisms of Change in the Patient	N/A
Completed	`NCT03308344` - Mindfulness Training in Military Spouses	N/A
Recruiting	`NCT06029348` - Cerebrovascular Health and Resilience in Midlife	N/A
Completed	`NCT05869006` - The Effect of Designed SIA Instrument Supported Interpersonal Relations-Based Group Practice on Psychological Well-Being and Creativity	N/A
Completed	`NCT04484649` - Sleeping Healthy/Living Healthy Development	N/A

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.