Flower Print Activity Applied to the Elderly in the Nursing Home

October 31, 2023 updated by: Hacer Gok Ugur, T.C. ORDU ÜNİVERSİTESİ

The Effect of Flower Printing Activity Applied to the Elderly in the Nursing Home on the Anxiety Levels of the Elderly: A Single-Blind Randomized Controlled Study

This research will be carried out in order to determine the effect of the flower pressure activity applied to the elderly in the nursing home on the anxiety levels of the elderly.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This research will be carried out in order to determine the effect of the flower pressure activity applied to the elderly in the nursing home on the anxiety levels of the elderly.

Hypotheses H0 = Flower pressure activity applied to the elderly in the nursing home does not affect the anxiety level of the elderly.

H1= Flower pressure activity applied to the elderly in the nursing home reduces the anxiety level of the elderly.

Study Type

Interventional

Enrollment (Actual)

42

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 Locations

  • Turkey
    • Altınordu
      • Ordu, Altınordu, Turkey, 52000
        • Hacer GÖK UĞUR

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

  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Has no physical handicap that may hinder the activity of flower printing,
  • No vision or hearing loss that may hinder the activity of flower printing,
  • Open to communication and cooperation,
  • The elderly who volunteer to participate in the study will be included in the study.

Exclusion Criteria:

  • Have a serious medical disability,
  • Having a serious psychiatric diagnosis,
  • Severely demented and
  • The elderly who do not want to continue the research will be excluded from the research.

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: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Control group
Other: Routine activities in nursing home
Control group
Experimental: Experimental group
Other: flower printing activities for the elderly
Experimental group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Geriatric Anxiety Scale
Time Frame: day 0 and day 30
The scale developed by Pachana et al. (2007) was adapted to Turkish by Pamir Akın (2010). The Geriatric Anxiety Inventory (GAS) aims to measure anxiety symptoms in the elderly in a dimensional way. The basic psychometric feature of the scale is that it can differentiate both the anxious/non-anxious group and the group with/without generalized anxiety disorder. The cut-off point of the scale for generalized anxiety disorder was determined as 10/11. Accordingly, the scale; "anxiety symptoms and generalized anxiety disorder > 10; only anxiety symptoms < 10". There is no reverse coded item in the scale, which consists of 20 items and is scored over two dimensions: "I agree" and "I do not agree". Accordingly, 1 point is given for the "agree" option and 0 points for the "disagree" option. Therefore, the scores obtained from the scale can vary between 0 and 20.
day 0 and day 30

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

T.C. ORDU ÜNİVERSİTESİ

Investigators

  • Principal Investigator: Hacer GÖK UĞUR, Assoc. Prof., Ordu Univercity

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 (Actual)

March 1, 2023

Primary Completion (Actual)

April 30, 2023

Study Completion (Actual)

June 1, 2023

Study Registration Dates

First Submitted

December 12, 2022

First Submitted That Met QC Criteria

April 27, 2023

First Posted (Actual)

April 28, 2023

Study Record Updates

Last Update Posted (Actual)

November 1, 2023

Last Update Submitted That Met QC Criteria

October 31, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 1Ordu

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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