Parrot Therapy on Pain During Venous Blood Collection in Individuals With Chronic Diseases
CompletedNot applicableNCT07241780
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
This double-blind randomized controlled trial was conducted to comparatively evaluate the effectiveness of live parrot, robotic parrot, and parrot picture therapies on pain during venipuncture in adults with chronic illness.
Study details
- Official title
- The Effect of Live and Non-Living Parrot Therapy on Pain During Venous Blood Collection in Individuals With Chronic Diseases: A Double-Blind Randomized Controlled Study
- Conditions
- Interventions
- Other: Live Parrot therapy (Pet therapy)
- Other: Robotic Parrot therapy (Pet therapy)
- Other: Picture Parrot therapy (Pet therapy)
- Sponsor
- Karadeniz Technical University
- Collaborators
- Gümüşhane Universıty
- Start date
- 2024-07-02
- Primary completion
- 2024-07-09
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- Turkey (Türkiye)
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Individuals aged 18 years or older, * Literate, * Able to communicate verbally, * Without vision/hearing/speech problems, * With at least 6 months of chronic disease, * With a single venous access point, and who gave consent were included. Exclusion Criteria: * Refusal to give consent, * Psychiatric diagnosis, * Hemodynamic instability, * Presence of Chronic Obstructive Pulmonary Disease/Asthma, * Chronic disease duration of less than 6 months.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07241780