Effects of Animal Assisted Activity on Biobehavioral Stress Responses of

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Psychosocial Stress

See also
Status	Clinical Trial	Phase
Completed	`NCT02997852` - Biobehavioral Effects of Therapy Dog Visitation in Elderly Intensive Care Unit Patients: A Pilot and Feasibility Study	N/A
Recruiting	`NCT01445015` - Stress Management Intervention in Inner City Adolescents With Asthma	Phase 2
Withdrawn	`NCT02002780` - Recognizing and Treating Psychosocial Stress Among Children With Complex Heart Problems	Phase 2
Recruiting	`NCT04324190` - DIgital Online SuPport for COVID-19 StrEss	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT02997852 - Biobehavioral Effects of Therapy Dog Visitation in Elderly Intensive Care Unit Patients: A Pilot and Feasibility Study

N/A

Recruiting

NCT01445015 - Stress Management Intervention in Inner City Adolescents With Asthma

Phase 2

Withdrawn

NCT02002780 - Recognizing and Treating Psychosocial Stress Among Children With Complex Heart Problems

Phase 2

Recruiting

NCT04324190 - DIgital Online SuPport for COVID-19 StrEss

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

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.

NCT number	NCT03017027
Study type	Interventional
Source	The University of Texas Health Science Center, Houston
Contact
Status	Completed
Phase	N/A
Start date	March 2015
Completion date	January 2016

Effects of Animal Assisted Activity on Biobehavioral Stress Responses of Hospitalized Children: A Randomized Control Trial

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms