- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07296380
Manual Therapy Behavior Scale in Physiotherapists
Development of a Manual Therapy Application Behavior Scale Among Physiotherapists: A Validity and Reliability Study
Study Overview
Status
Conditions
Detailed Description
Manual therapy is an evidence-based intervention method based on manual techniques widely used by physiotherapists in the treatment of musculoskeletal disorders. However, clinicians' decisions to implement manual therapy are influenced by multidimensional factors such as personal attitudes, professional beliefs, institutional policies, educational experiences, and the culture of clinical practice. The use of behavior-based theoretical models is recommended to evaluate these factors together.
The Theory of Planned Behavior (Ajzen, 1991) is a powerful approach that explains individuals' intentions to perform a specific behavior through variables such as attitude, subjective norm, perceived behavioral control, and intention. Although this theory is frequently used to understand the clinical decision-making processes of healthcare professionals, there is no valid and reliable measurement tool in Turkey for measuring behavior toward manual therapy practices.
This study will develop a new scale adapted to Turkish culture to assess physiotherapists' manual therapy practices in a theoretically based manner. The research will consist of three phases:
Item Development Phase:
The item pool generated through the literature review will be presented to expert physiotherapists.
Expert Panel/Delphi Phase:
Experts will evaluate the items based on content validity, and items will be revised or removed based on consensus. In this phase, the Content Validity Index (CVI) and Content Validity Ratio (CVR) will be evaluated.
Statistical Analysis Phase:
The final scale will be administered online to physical therapists.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Denizli
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Denizli, Denizli, Turkey (Türkiye), 20160
- Pamukkale University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Be actively working as a physiotherapist in Turkey (public/private hospital, university hospital, private clinic, etc.)
- Have received basic training in manual therapy or have clinical practice experience
- Be a healthy adult aged 22 or over
- Be able to read and understand Turkish (the survey language is Turkish)
- Agree to participate in the study voluntarily and provide individual informed consent
Exclusion Criteria:
- Professionals working in healthcare fields other than physiotherapy
- Physiotherapists without manual therapy experience
- Participants who complete the survey form incompletely, incorrectly, inconsistently, or provide duplicate entries
- Individuals who refuse to provide informed consent
- Individuals who withdraw their voluntary consent during the research process
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Phsysiotherapists
Healthy adult physiotherapists who are actively working in public or private healthcare institutions or university clinics in Turkey and have received training or basic practical experience in manual therapy.
Participation is voluntary, and no clinical intervention will be performed.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Manual Therapy Application Behavior Scale for Physiotherapists
Time Frame: One-time evaluation during the data collection period
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"Manual Therapy Application Behavior Scale in Physiotherapists" is a 7-point Likert-type (1 = Strongly disagree, 7 = Strongly agree) self-report scale developed based on Ajzen's Planned Behavior Theory.
Higher scores reflect more positive attitudes, stronger subjective norms, higher perceived behavioral control, and higher behavioral intentions among physical therapists toward manual therapy.
Construct validity will be assessed using internal consistency (Cronbach's alpha), item-total correlations, test-retest reliability, and confirmatory factor analysis.
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One-time evaluation during the data collection period
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- E-60116787-020-789576
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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