- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07500402
THE EFFECT OF GARDENING ON PSYCHOLOGICAL WELL-BEING AND CARE AMONG NURSING HOME CARE STAFF
March 24, 2026 updated by: Simge Tombul, Ordu University
THE EFFECT OF GARDENING ACTIVITIES APPLIED TO CARE STAFF IN NURSING HOMES ON PSYCHOLOGICAL WELL-BEING AND CARE: A MIXED METHODS STUDY
This study will be conducted to evaluate the effects of horticultural activities applied to nursing home care staff on their psychological well-being and caregiving, and to examine in depth the care staff's views on horticultural activities.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
41
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: SİMGE TOMBUL
- Phone Number: +90 553 754 28 52
- Email: simgetombul@gmail.com
Study Contact Backup
- Name: HACER GÖK UĞUR, Prof. Dr.
- Phone Number: 6410 +90 452 226 52 00
- Email: hacer32@gmail.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Care staff working in active care services at a nursing home, Who have been working at a nursing home for at least one year (Maunder et al., 2022), Who are open to communication and collaboration, And who are willing to participate in the study will be included in the research.
Exclusion Criteria:
- Those on leave, on sick leave, or undergoing a job reassignment during the research process Care staff with any physical or mental disabilities that could prevent them from participating in gardening activities will not be included in the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: intervention group
Horticultural activity group
|
In this study, care staff will participate in gardening activities once a week for 8 weeks, for an average of 60 minutes per session.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Psychological Well-Being Scale
Time Frame: Day 0-Month 2
|
The validity and reliability study of the scale developed by Butler and Kern (2016) to assess individuals' levels of well-being was conducted by Demirci et al. (2017).
The scale consists of 15 items, 8 dummy items, and 5 subscales.
The scale's name is derived from the initial letters of the subscales in English.
|
Day 0-Month 2
|
|
Bakas Caregiving Impact Scale
Time Frame: Day 0-Month 2
|
The scale was developed by Bakas (1999), and its validity and reliability in Turkish were established by Can and Cavlak in 2010.
The scale is a Likert-type scale ranging from 1 to 7. The scale consists of a total of 15 questions scored between +3 (best) and -3 (worst) and reflects both the positive and negative effects of care.
A score ranging from a minimum of 15 to a maximum of 105 is possible.
As the scale score increases, it is interpreted as a "positive change"; as the score decreases, it is interpreted as a "negative change."
The Cronbach's alpha value for the scale was found to be 0.90.
|
Day 0-Month 2
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
May 1, 2026
Primary Completion (Estimated)
July 1, 2026
Study Completion (Estimated)
December 1, 2026
Study Registration Dates
First Submitted
March 24, 2026
First Submitted That Met QC Criteria
March 24, 2026
First Posted (Actual)
March 30, 2026
Study Record Updates
Last Update Posted (Actual)
March 30, 2026
Last Update Submitted That Met QC Criteria
March 24, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ORDU-SABE-ST-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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