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Measuring Effects of Contact to Dogs

Measuring the Effects of Different Intensities of Contact to Dogs

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04696419
Enrollment
46
Registered
2021-01-06
Start date
2020-10-01
Completion date
2021-10-01
Last updated
2021-11-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavioural Responses to Contact With Dogs, Physiological Responses to Contact With Dogs, Psychological Responses to Contact With Dogs

Keywords

Animal-assisted therapy, Non-invasive measure, Human-animal contact

Brief summary

The study aims to identify and quantify objective non-invasive measures of the immediate effect of contact with dogs in a standardized experimental setup. Employing a within-subject design, the study includes healthy participants that are exposed to three different levels of contact to a dog compared with a no-dog control condition while obtaining measures of both physiological, behavioral, and psychological effects.

Detailed description

Using a within-subjects design, we will compare four standardised and controlled test situations with different levels of dog contact: 1\) visual (V), 2) tactile and visual (TV), 3) tactile, visual, interaction (TVI), and 4)control (C). The participants will be subjected to all four test situations on the same day, and will be randomly allocated to test order. On the test day, we collect background information and baseline measures for the participants (baseline period, duration: 50 minutes), whereafter they rest for 30 minutes (pre-intervention rest period). After this the participants are subjected to the four test situations (10 minutes each) that are followed by rest intervals (30 minutes each). The participants' interaction with the dog during the 10-minute test situations are standardised according to the specific contact treatment. Most physiological and all behavioural measures are recorded continuously throughout each test in order for us to link the dosage of dog (the different levels of contact) with the psychological responses and some physiological measures obtained before an after each test situation. Below is shown the exact time schedule of the test day, that we refer to when describing the outcome measures. The baseline period (30 minutes) is not included in the total test period (total duration= 190 minutes), that consist of a pre-intervention and intervention period. * Baseline period (50 minutes - not part of total test period) * Pre-intervention period (start, t=0 minutes; end t= 30 minutes) * Test situation 1 (start, t=30 minutes; end, t=40 minutes) * Rest period 1 (start, t=40 minutes, end, t= 70 minutes) * Test situation 2 (start, t=70 minutes; end, t=80 minutes) * Rest period 2 (start, t=80 minutes, end, t= 110 minutes) * Test situation 3 (start, t=110 minutes; end, t=120 minutes) * Rest period 3 (start, t=120 minutes, end, t= 150 minutes) * Test situation 4 (start, t=150 minutes; end, t=160 minutes) * Rest period 4 (start, t=160 minutes, end, t= 190 minutes)

Interventions

OTHERDifferent intensities of contact to dogs

Each subject is exposed to four test situations of 10 minutes. Three situations with increasing intensity of dog contact, and one control test situation with no contact to a dog. The order of the test situations is random and with 30 minute washout in-between

Sponsors

University of Aarhus
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Randomised within-subject design. Each subject is exposed to three different levels of contact with a dog and a control situation in randomised order.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Normal cognitive functioning and physical movement * Ability to speak and read Danish

Exclusion criteria

* Known medical, psychiatric or neurological disease * Use of psychotropic medications * Frequent use of pain medication * Use of illegal psychotropic drugs * Known allergies to dogs

Design outcomes

Primary

MeasureTime frameDescription
The State-Trait Anxiety Inventory (STAI)Baseline: Measured at onset of the 30 minute pre-intervention period preceeding the first of the four test situations (t=0 minutes)State anxiety is measured with the STAI-scale (minimum score= 20, maximum score= 80, and a lower score indicates a high anxiety level)
Visual analogue scales measuring perceived psychological and physiological effects of each of the four test situationsTest periods: Measured immediately following the first test situations: t=40 minutesTest persons fill in a visual analoque scale. Minimum value -100 (very negative effect) and maximum value 100 (very positive effect), and 0 being neutral.
Visual analogue scales measuring perceived psychological and physiological effects of of the test day including, including all four test situationsAfter last resting period: Measured at the end of the last resting period, following the last of the four test situations, t=190 minutesTest persons fill in a visual analoque scale. Minimum value -100 (very negative effect) and maximum value 100 (very positive effect), and 0 being neutral.
Salivary cortisolBaseline: Measured at onset of the 30 minute pre-intervention period preceeding the first of the four test situations (t=0 minutes)Saliva is obtained from the testperson with a cotton swab which is chewed for one minute
Physiological measure, heart rateMeasured continuously throughout the total test period of 190 minutes (through the pre-intervention period, the four test situations and all resting periods)The test person wears self-adhesive electrodes and the heart rate is measured non-invasively,
Salivary oxytocinBaseline: Measured at onset of the 30 minute pre-intervention period preceeding the first of the four test situations (t=0 minutes)Saliva is obtained from the testperson with a cotton swab which is chewed for one minute
The Positive and Negative Affect Schedule (PANAS)Baseline: Measured at onset of the 30 minute pre-intervention period preceeding the first of the four test situations (t=0 minutes)Positive and negative affect is measured with the PANAS scale, where the person scores whether or not they experience each of 20 emotions on a 5-step scale from very little /not at all to extremely much. The emotions differ in valens.
Physiological measure, blood pressureBaseline: Measured at onset of the 30 minute pre-intervention period preceeding the first of the four test situations (t=0 minutes)Blood pressure is measured manually with a blood pressure monitor with a blood pressure cuff
Physiological measure, heart rate variablilityMeasured continuously throughout the total test period of 190 minutes (through the pre-intervention period, the four test situations and all resting periods)Heart rate variability is calculated from heart rate data
Physiological measure, galvanic skin responseMeasured continuously throughout the total test period of 190 minutes (through the pre-intervention period, the four test situations and all resting periods)The test person is fitted with electrodes on two fingers and galvanic skin response is measured non-invasively,
Visual analogue scales measuring expected psychological and physiological effects of the test day including, including all four test situationsBaseline: Measured at onset of the 30 minute pre-intervention period preceeding the first of the four test situations (t=0 minutes)Test persons fill in a visual analoque scale. Minimum value -100 (very negative effect) and maximum value 100 (very positive effect), and 0 being neutral.
Visual analogue scales measuring expected psychological and physiological effects of each of the four test situationsTest periods: Measured immediately preceeding the first test situation: t=30 minutesTest persons fill in a visual analoque scale. Minimum value -100 (very negative effect) and maximum value 100 (very positive effect), and 0 being neutral.

Secondary

MeasureTime frameDescription
Quantitative behavioural measures - duration of behavioural elementsMeasured continuously throughout the total test period of 190 minutes (through the pre-intervention period, the four test situations and all resting periods)A video recording of the test persons behaviour is analysed for the duration (seconds) of predefined behavioural elements Postures: sitting, standing walkning Touching the dog: being in physical contact with the dog with tha hand or another part of the body Looking at the dog: Having head turned towards the dog Talking to the dog: Directing talk directly at the dog, as opposed to the person present
Quantitative behavioural measures - frequencies of behavioural elementsMeasured continuously throughout the total test period of 190 minutes (through the pre-intervention period, the four test situations and all resting periods)A video recording of the test persons behaviour is analysed for frequency of predefined behavioural elements Postures: sitting, standing walkning Touching the dog: being in physical contact with the dog with tha hand or another part of the body Looking at the dog: Having head turned towards the dog Talking to the dog: Directing talk directly at the dog, as opposed to the person present

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026