- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06807476
Turkish of the Acupuncture Readiness Attitude Scale
Turkish Validity and Reliability of the Acupuncture Readiness Attitude Scale
Objectives: Acupuncture is often used to promote health and well-being, relieve pain, and treat a variety of medical conditions. Acupuncture is believed to work by stimulating the body's natural healing processes, and it is important that individuals are prepared to receive acupuncture. The study aims to examine the Turkish validity and reliability of the Acupuncture Readiness Attitude Scale, which will be used to evaluate the well-being levels of haptonomy and haptotherapy practices in women.
Design: The study was methodological type. Methods: The study conducted between Aug 9 and December 30, 2024, with 510 women who volunteered to participate by sharing forum pages on social media (Facebook, Instagram) via the web. Data were collected using a personal information form, including sociodemographic and obstetric characteristics and the Acupuncture Readiness Attitude Scale.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Bartın, Turkey, 74010
- Bartın University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Individuals who are over the age of 18,
- Live in Turkey,
- Use social media, and agree to participate in the study will be included in the study.
Exclusion Criteria:
- Women who do not know how to read or write Turkish,
- Have hearing or vision problems or mental disabilities,
- Do not have social media,
- Do not volunteer to participate in the study will not be included in the study.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Validity and reliability
|
The scale consists of 40 items and four sub-dimensions, and is scored according to a 5-point Likert rating scale (ranging from "Strongly Disagree" (Score = 1 point) to "Strongly Agree" (Score = 5 points)). The scale evaluates the healthy/patient individual's readiness attitude level towards acupuncture, personal beliefs, preferences and experiences. The score received per sub-dimension varies between a minimum of 10 and a maximum of 50 points. The average cut-off score per sub-dimension is 25. The higher the score (above the average cut-off score), the more open the healthy/patient individual is to acupuncture. Sub-dimensions: Sub-Dimension 1 (Items 1-10): Willingness to Try Acupuncture Sub-Dimension 2 (Items 11-20): Belief in the Effectiveness of Acupuncture Sub-Dimension 3 (Items 21-30): Comfort in the Acupuncture Sub-Dimension 4 (Items 31-40): Concerns and Preferences |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Acupuncture Readiness Attitude Scale
Time Frame: 1 day
|
The scale consists of 40 items and four sub-dimensions, and is scored according to a 5-point Likert rating scale (ranging from "Strongly Disagree" (Score = 1 point) to "Strongly Agree" (Score = 5 points)).
The scale evaluates the healthy/patient individual's readiness attitude level towards acupuncture, personal beliefs, preferences and experiences.
The score received per sub-dimension varies between a minimum of 10 and a maximum of 50 points.
The average cut-off score per sub-dimension is 25.
The higher the score (above the average cut-off score), the more open the healthy/patient individual is to acupuncture.
|
1 day
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2024-SBB-0605
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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