Actively Recruiting
Medical Affairs Pharmaceutical Physician Work-related Quality of Life (MAPPWrQoL) Instrument Development and Patient Registry (MAPPWrQoLReg)
Led by Medialis Ltd. · Updated on 2023-10-23
180
Participants Needed
1
Research Sites
256 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Existing evidence has shown that medical affairs pharmaceutical physicians (MAPPs), are a core function within the pharmaceutical industry. Despite their expertise, there are ongoing concerns about recognition and respect for the MAPP's role within the pharmaceutical industry. Anecdotal evidence further suggests that this lack of recognition and respect for the valuable contribution of this specialised group of medical doctors may impact their quality of life, resulting in stress, anxiety, depression and occupational burnout. Hence, participants are likely to use NHS services as patients, when experiencing the physical, mental, and emotional issues associated with occupational burnout, an internationally recognised condition (ICD-11 code QD85) resulting from chronic occupational stress. This observational study will recruit participants to contribute data to creating a MAPP work-related participant-reported outcome measure on the impact of work-related performance on quality of life (QoL). The created MAPP work-related participant-reported measure will be used longitudinally with study participants to measure their QoL monthly for 12 months. In total, up to 180 Medical Affairs Pharmaceutical Physicians are expected to be recruited to the study. The study will be conducted in two main phases, involving three online surveys.
CONDITIONS
Official Title
Medical Affairs Pharmaceutical Physician Work-related Quality of Life (MAPPWrQoL) Instrument Development and Patient Registry (MAPPWrQoLReg)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Qualified as a Medical Affairs Pharmaceutical Physician with a medical degree
- Current or previous work experience within a pharmaceutical company
- Able to provide informed consent
- Able to read, write, and converse in English
- Able to comply with the study schedule
- 18 years of age or older
You will not qualify if you...
- Not working or having worked in the pharmaceutical industry as a Medical Affairs Pharmaceutical Physician
- Unable to comply with the study schedule
- Unable to read, write, or converse in English
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Medialis
Oxford, United Kingdom, OX16 0AH
Actively Recruiting
Research Team
O
Omolade Femi-Ajao, PhD
CONTACT
R
Ravi Jandhyala
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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