The Effect of Therapeutic Touch on Sleep and Anxiety
1 other identifier
interventional
68
1 country
1
Brief Summary
The aim of this study is to determine the effect of the therapeutic touch applied to the sleep patterns of individuals aged 65-85 years with chronic diseases who are treated in the Neurology Intensive Care Unit of Ankara City Hospital, taking into account the circadian cycle.The type of the research is the experimental model with pre-test and post-test control group.Ankara City Hospital has included the research population in the last year. It will consist of 1593 patients between the ages of 65-85 who are hospitalized in the Neurology Intensive Care Unit.Experimental and control groups will be created with simple randomization in randomization.The data were obtained from the socio-demographic characteristics form and the sleep pattern form developed by the researcher. will be collected with
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2022
CompletedFirst Submitted
Initial submission to the registry
April 28, 2022
CompletedFirst Posted
Study publicly available on registry
May 6, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 23, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 15, 2023
CompletedResults Posted
Study results publicly available
April 13, 2026
CompletedApril 13, 2026
April 1, 2022
1.1 years
April 28, 2022
November 11, 2023
March 24, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Visual Analogue Scale
The Visual Analogue Scale - Anxiety Subtest (VAS-Anxiety) was used to measure anxiety levels. Scores ranged from 0 to 100, where 0 represents no anxiety and 100 represents the highest possible anxiety. Higher scores indicate a worse outcome. Patients marked their anxiety level on the scale, and this score was recorded as the outcome measure.
pretest (Measurements taken during the initial consultation)
Comparison of Sleep Duration and Sleep Onset Difficulties by Group at Measurement Times (Sleep Duration)
In this measurement, the sleep duration was recorded as subjective data by the researcher. (Calculated based on the intended bedtime and wake-up time)
pretest (Measurements taken during the initial consultation)
Secondary Outcomes (2)
Visual Analogue Scale
posttest (three weeks after the pre-test)
Comparison of Sleep Duration and Sleep Onset Difficulties by Group at Measurement Times (Sleep Duration)
posttest (three weeks after the pre-test)
Study Arms (2)
The effect of therapeutic touch on sleep patterns of elderly patients
EXPERIMENTALThe important effects of the therapeutic approach made by the researcher to the elderly patients hospitalized in the intensive care unit will be evaluated.
Determining the sleep pattern of the Control Group
NO INTERVENTIONIt will be evaluated whether there is a change in sleep patterns without intervention in the control group.
Interventions
Therapeutic Touch (TT) is an evidence-based holistic treatment method in which universal energy is used intentionally and with compassion for a specific purpose, in order to contribute to one's balance and recovery.In a world dominated by technology, one can lose touch with our inner self. We lose our intuitive abilities for beautiful everyday sensations of nature, the surrounding environment, and various visual and auditory elements. The Therapeutic Touch is an ancient Ayurvedic self-massage technique that connects your body to your soul.It is also used in therapeutic communication. Therapeutic communication is the process of influencing and being influenced by one another. It consists of individual-centered, purposeful, planned, effective and satisfying actions.
Eligibility Criteria
You may qualify if:
- Being in the age range of 65-85 years
- Having a Chronic Disease
- The patient is receiving treatment at the hospital
You may not qualify if:
- Not in the age range of 65-85 years
- Not being able to communicate (being intubated, having hearing impairment, etc.)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Berna Bayır
Karatay, Konya, 42020, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Results Point of Contact
- Title
- Dr. Berna BAYIR
- Organization
- KTO Karatay University
Study Officials
- PRINCIPAL INVESTIGATOR
Berna Bayır
KTO Karatay University
Publication Agreements
- PI is Sponsor Employee
- No
- Restrictive Agreement
- No
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 28, 2022
First Posted
May 6, 2022
Study Start
January 1, 2022
Primary Completion
January 23, 2023
Study Completion
August 15, 2023
Last Updated
April 13, 2026
Results First Posted
April 13, 2026
Record last verified: 2022-04
Data Sharing
- IPD Sharing
- Will not share