- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05820022
Scientific Research Barriers by Gender and Other Characteristics in Physiatry
July 7, 2023 updated by: Mustafa Hüseyin Temel, Uskudar State Hospital
Evaluating Scientific Research Barriers by Gender and Other Characteristics From the Perspective of Physiatrists in Turkey: A Multicenter Survey Study
The ever-increasing population and life expectancy worldwide lead to a higher prevalence of physical disabilities and diseases, which increases the need for physical medicine and rehabilitation research.
In our study, we aimed to evaluate various aspects of the barriers, particularly gender disparities, faced by physical medicine and rehabilitation professionals who wish to conduct scientific research.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Physicians in physical medicine and rehabilitation must also put in tremendous effort and manage their time meticulously to contribute to scientific research (SR).
Research requires knowledge, experience, and institutional support, such as financial incentives, technical facilities, and trained personnel.
In this field, research productivity is increasingly important due to the rising prevalence of conditions such as age-related disability and chronic pain, which put pressure on the healthcare system and affect people's quality of life.
Turkey's publication productivity in physical medicine and rehabilitation has also increased steadily in recent years, with a significant number of articles published between 2015 and 2020.
However, gender disparities in academic leadership positions persist in this field as well, with women lagging behind men in the number of scientific publications.
While bibliometric studies are useful for assessing the current state of scientific performance, survey studies are necessary to identify obstacles that deter researchers and increase research productivity.
Unfortunately, few studies have used this approach in physical medicine and rehabilitation, and no such study has been conducted in Turkey.
Study Type
Observational
Enrollment (Actual)
254
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: Mustafa H Temel
- Phone Number: +905342714872
- Email: mhuseyintemel@gmail.com
Study Contact Backup
- Name: Fatih Bağcıer, M.D.
- Phone Number: +905542429042
- Email: bagcier_42@hotmail.com
Study Locations
-
-
Üsküdar
-
Istanbul, Üsküdar, Turkey, 34000
- Uskudar State Hospital
-
-
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
Sampling Method
Non-Probability Sample
Study Population
Physical medicine and rehabilitation physicians who consented to participate in the study.
Description
Inclusion Criteria:
- Being a physical medicine and rehabilitation physician.
- Giving consent to participate in the study.
Exclusion Criteria:
- Not giving consent to participate 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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Physical Medicine and Rehabilitation Specialists
Physical medicine and rehabilitation specialists
|
This scale was prepared after a detailed literature review and sent to five physiatrists for review and feedback.
It consists of 21 items with Likert-type responses and two open-ended questions.
It is designed to measure the barriers that individuals or groups face in conducting research.
The scale includes a list of potential barriers and asks respondents to rate the extent to which they experience each barrier.
Examples of barriers that may be included in such a scale could include lack of funding, limited access to resources or equipment, time constraints, difficulty finding participants or accessing data, institutional or administrative hurdles, and so on.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Research Barriers Scale
Time Frame: 1 day
|
This scale was prepared after a detailed literature review and sent to five physiatrists for review and feedback.
It consists of 21 items with Likert-type responses and two open-ended questions.
It is designed to measure the barriers that individuals or groups face in conducting research.
The scale includes a list of potential barriers and asks respondents to rate the extent to which they experience each barrier.
Examples of barriers that may be included in such a scale could include lack of funding, limited access to resources or equipment, time constraints, difficulty finding participants or accessing data, institutional or administrative hurdles, and so on.
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mustafa H Temel, M.D., Uskudar State Hospital
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)
May 1, 2023
Primary Completion (Actual)
June 15, 2023
Study Completion (Actual)
June 15, 2023
Study Registration Dates
First Submitted
April 6, 2023
First Submitted That Met QC Criteria
April 6, 2023
First Posted (Actual)
April 19, 2023
Study Record Updates
Last Update Posted (Actual)
July 10, 2023
Last Update Submitted That Met QC Criteria
July 7, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- Barrier1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
IPD will be shared upon reasonable request by the principal investigator.
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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