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Comparing the Stress-Reducing Effects of a Robotic Pet and a Weighted Toy

U

University of Auckland, New Zealand

Status

Not yet enrolling

Conditions

Stress

Treatments

Device: Paro Robotic Companion Seal
Device: Weighted Sensory Toy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this trial is to learn whether interacting with a robotic pet (Paro) or holding a weighted sensory toy can reduce stress in healthy adults after an acute stressful experience. The main questions it aims to answer are:

  • Does interacting with Paro or holding a weighted toy lower self-reported stress and anxiety levels?
  • Does interacting with Paro or holding a weighted toy lower physiological markers of stress, such as heart rate and blood pressure?

Researchers will compare interaction with Paro (robotic pet), interaction with a weighted sensory toy and a control group with no intervention to see which method is most effective in reducing stress.

Participants will:

  1. Complete a stress induction task (Trier Social Stress Test);
  2. Be randomly assigned to interact with Paro, hold a weighted toy, or sit quietly without intervention;
  3. Have their heart rate and blood pressure measured;
  4. Complete surveys about their stress, anxiety and mood before and after the intervention.

Full description

The study investigates the immediate effectiveness of interacting with an interactive robotic pet (Paro, a robotic seal) or a weighted sensory modulation toy for reducing acute stress and anxiety. It aims to determine the comparative efficacy of these interventions relative to a control condition involving quiet relaxation. Participants will be randomly assigned to one of three experimental conditions: interaction with Paro, interaction with a weighted sensory toy, or a control group with no intervention.

All participants will first complete baseline measurements, including self-reported anxiety and stress assessments using validated instruments (State-Trait Anxiety Inventory, Positive and Negative Affect Schedule, and Visual Analog Scale), as well as physiological indicators of stress (heart rate and blood pressure). Subsequently, participants will undergo the Trier Social Stress Test (TSST), a validated procedure involving a brief public speaking task and mental arithmetic performed under evaluative conditions designed to induce moderate stress. Following the stress induction, participants will repeat stress and anxiety assessments and physiological measurements. They will then engage in their assigned intervention for 15 minutes. Post-intervention measurements of stress and anxiety, physiological markers, and perceived enjoyment/ engagement will be collected. Participants will also provide qualitative feedback regarding their intervention experiences.

Enrollment

51 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • over 18 years old
  • fluent in English
  • free from diagnosed anxiety or stress-related disorders

Exclusion criteria

  • cardiovascular conditions that may affect heart rate and blood pressure measurements
  • existing anxiety disorders or panic disorders.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

51 participants in 3 patient groups

Paro Robot Interaction
Experimental group
Description:
Participants will interact with Paro, a robotic companion seal, for 15 minutes following a stress induction task. Paro responds to touch and sound.
Treatment:
Device: Paro Robotic Companion Seal
Weighted Toy Interaction
Experimental group
Description:
Participants will hold and interact with a weighted sensory toy for 15 minutes following a stress induction task. The weighted toy provides deep pressure stimulation for calming effects.
Treatment:
Device: Weighted Sensory Toy
Control Group (No Intervention)
No Intervention group
Description:
Participants will sit quietly for 15 minutes without any intervention following a stress induction task. This group allows natural recovery from stress without external aids.

Trial contacts and locations

1

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Central trial contact

Nina Akulova

Data sourced from clinicaltrials.gov

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