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Physicians & Patients Reported Outcomes

Outcomes research (also often called real world evidence) is used to establish and measure the link between treatment and actual outcomes. This is achieved by measuring quality of life and satisfaction as reported by the patients but also by understanding how healthcare providers prescribe drugs and how these drugs are performing in the real world. It provides evidence-based guidance on how to improve care but also enables evaluation and generates evidence to define, substantiate, and communicate the value treatment to various stakeholders.

At Medicys, we are experts at collecting such outcomes from physicians and patients for the following types of studies

Prospective Non-Interventional studies (NIS)

Where our large network of physicians enrols patients a priori, following certain eligibility criteria and with the potential to follow them multiple times until the end of the study. The assignment of the patient to a particular therapeutic strategy falls within current practice and the prescription of the medicine is clearly separated from the decision to include the patient in the study. Each NIS seeks to measure product or intervention specific primary and secondary outcomes.
the required sample?

Case Record Forms (CRF) studies

Where Medicys recruit physicians to undertake chart reviews and completion of (usually) on-line case record forms. The number of cases reviewed can range from quite small numbers for very rare conditions to many hundreds for more common conditions.

Exit interviews

Where our expert healthcare moderators interview trial patients, usually at the last visit, or very soon after. Exit interviews are a valuable method for understanding the patient experience, informing measurement strategy and aiding interpretation of patient reported outcomes. Medicys has developed secure, tried and tested digital methods to lessen the logistical burden on investigator and sites.

Implementation science studies

Where we assist clients identify and address the barriers that slow or halt the uptake of proven health interventions and evidence based practices by recruiting and interviewing healthcare professionals and patients.

PROMs/ PREMs development and validation

We help clients who specialise in developing Patient Reported Outcomes Measures and Patient Reported Experience Measures by recruiting patients for qualitative interviews to identify statements relating to the impact of the condition on the lives of the patients and produce draft measures. We also assist in the cognitive debriefing phase by testing the measures with a fresh sample of patients before moving to the validation phase in which the measure is tested with a much larger sample of patients.

Related Work

physicians and patients reported outcomes

Therapy Area: Haematology
Topic: AML

Acute Myeloid Leukaemia

Respondent Type: Hematologists, Onco-hematologists

To understand treatment behavior in tnAM

Countries:
Sample Size: 20
Methodology: 55-minute online survey followed by 45-minute Web Assisted Telephone Depth Interviews (WATDIs)
Services Delivered: Recruitment, translations, moderation, sim trans, content analyses

physicians and patients reported outcomes

Therapy Area: Haematology
Topic: CLL

Chronic Lymphocytic Leukaemia

Respondent Type: Haematologists

To gain an understanding and to compare treatment patterns and outcomes in CLL

Countries:
Sample Size: 50
Methodology: 45-minute online survey
Services Delivered: Recruitment

physicians and patients reported outcomes

Therapy Area: Respiratory diseases
Topic: Asthma
Respondent Type: Parents of children with severe asthma

To understand the experiences of children and their families who live with severe asthma and to get reactions to some draft communications materials.

Countries:
Sample Size: 16
Methodology: 75 minute Web Assisted Telephone Depth Interviews (WATDIs)
Services Delivered: Recruitment

physicians and patients reported outcomes

Therapy Area: Urology
Topic: OAB

Overactive Bladder

Respondent Type: Patients with overactive bladder

To help gain a better understanding of patients experiences with overactive bladder or bladder symptoms, and the value of treatments for overactive bladder.

Countries:
Sample Size: 300
Methodology: Pilot Study: 20- 30 minute WATDI. 45 minute post- task. Main Study: 10-25 minute WATDI
Services Delivered: Recruitment

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