- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05067686
Health Professionals Perspective on Suicide
March 2, 2023 updated by: Syeda AYAT E ZAINAB Ali
Health Professionals Perspective on Suicide: A Study of Their Attitude, Challenges and Suicide Prevention
The aim is to investigate how health professionals view/respond towards suicidal patients, what was their attitude, experiences and difficulties/challenges they faced while dealing with suicidal patients (whether successful or unsuccessful), and what measures/methods are optimal or could be used to prevent suicide from the perspective of mental and non mental health professionals through concurrent mixed methods study approach.
Study Overview
Status
Recruiting
Study Type
Observational
Enrollment (Anticipated)
100
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: Syeda Ayat e Zainab Ali, PhD Scholar
- Phone Number: +923121319004
- Email: zai_nab1@hotmail.com
Study Contact Backup
- Name: Dr Tamkeen Saleem, PhD
- Phone Number: (00)92-(0)51-9019887
- Email: tamkeen.saleem@iiu.edu.pk
Study Locations
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-
Capital
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Islamabad, Capital, Pakistan, 44000
- Recruiting
- International Islamic University, Islamabad Pakistan
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Contact:
- Syeda Ayat e Zainab Ali, PhD Scholar
- Phone Number: +923121319004
- Email: zai_nab1@hotmail.com
-
Contact:
- Dr Tamkeen Saleem, PhD
- Phone Number: (00)92-(0)51-9019887
- Email: tamkeen.saleem@iiu.edu.pk
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-
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
25 years to 60 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Considering the study design (concurrent mixed methods), a sample size of sixteen health professionals from different specialties (n=4, Accident and Emergency, n=4 Medicine, n=4 Surgery, n=4 Mental Health) who are the front line clinicians dealing with suicidal behavior will be recruited for the qualitative study.
For the quantitative study, the sample will comprised of ninety (n=100) health professionals from respective departments (n=50, (Non Mental Health Professionals, n=50 Mental Health Professionals).
Data will be collected through purposive sampling technique.
Description
Inclusion Criteria:
- Health professionals having at least 1 year of experience in dealing with suicide cases irrespective of the outcome will be included.
- Qualification of Health professionals should be at least MBBS with permanent PMDCP registration.
- Health professionals who are willing to participate voluntarily and provide written informed consent will be included.
Exclusion Criteria:
- Health Professionals with prior and present history of psychiatric consultation will be excluded.
- Health Professionals without direct experience in handling suicidal patients will be excluded.
- Nurses and Paramedical staff will be excluded from 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 |
|---|
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Mental Health Professionals
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Non Mental Health Professionals
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Interview Protocol for Qualitative Study
Time Frame: Day 1
|
A interview protocol for qualitative study will comprised of detailed demographic sheet and open ended questions.
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Day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Understanding Suicidal Patients (USP) scale
Time Frame: Day 1
|
The Understanding Suicidal Patients (USP) scale (Samuelsson, Asberg, & Gustavsson, 1997) will be used to measure willingness to provide care to suicide attempters and to assess the professional's understanding and sympathy for these patients.
|
Day 1
|
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The Stigma of Suicide Scale (SOSS-SF)
Time Frame: Day 1
|
The Stigma of Suicide Scale (SOSS-SF) is a 16-item short form have been developed to examine attitudes towards "a prototypical person who completed suicide"
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Day 1
|
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Attitudes towards Suicide Scale
Time Frame: Day 1
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The scale is used to examine the respondents' opinions and attitudes towards suicide.
Factors measured by the scale are: (1) acceptability of suicide; (2) suicide as a sign of mental illness; (3) the belief that persons who commit suicide will be punished after death; (4) the opinion that suicidal people should communicate their problems; (5) the intention to hide past suicidal behavior; and (6) the opinion that suicide should be discussed and reported openly among friends or in the news.
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Day 1
|
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Attitudes towards Suicide Prevention Scale
Time Frame: Day 1
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Attitude toward suicide prevention scale is a 14-item, self-rated, 5-point Likert scale (Strongly agree to strongly disagree) will be used to asses attitudes towards suicide prevention.
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Day 1
|
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Difficulties in Suicidal Behaviors Intervention Questionnaire - Version for Psychologists and Doctors (DSBQ)
Time Frame: Day 1
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To assess the difficulties of health professionals when facing a patient who seeks help after a suicide attempt.
|
Day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Dr Tamkeen Saleem, PhD, International Islamic University, Islamabad, Pakistan
- Study Chair: Dr Michelle O'Reilly, PhD, University of Leicester and Leicestershire Partnership NHS Trust
- Study Chair: Dr Stefan M Schulz, PhD, University of Wuerzburg
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
October 1, 2021
Primary Completion (Anticipated)
March 29, 2023
Study Completion (Anticipated)
April 30, 2023
Study Registration Dates
First Submitted
September 24, 2021
First Submitted That Met QC Criteria
September 24, 2021
First Posted (Actual)
October 5, 2021
Study Record Updates
Last Update Posted (Estimate)
March 3, 2023
Last Update Submitted That Met QC Criteria
March 2, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LWL-HPPS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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