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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: Nephrology
Topic: CKD

Chronic Kidney Disease

Respondent Type: Patients

To better understand the experiences of people with CKD or ESKD.

Countries:
Sample Size: 30
Methodology: 60 minute Web Assisted Telephone Depth Interviews
Services Delivered: Recruitment

physicians and patients reported outcomes

Therapy Area: Gastroenterology
Topic: UC

Ulcerative Colitis

Respondent Type: Gastroenterologists

To better understand current practice in Ulcerative Colitis.

Countries:
Sample Size: 20 physicians and 660 PRFs
Methodology: 15 minute Online Opinion Survey and 30 minute PRF's
Services Delivered: Recruitment

physicians and patients reported outcomes

Therapy Area: Oncology
Topic: mRCC

metastatic Renal Cell Carcinoma

Respondent Type: Oncologists

To gain an understanding and to comparing treatment patterns (Targeted therapies or immunotherapy or inmuno-oncology) in metastatic Renal Cell Carcinoma (mRCC), for the development of marketing campaigns, educational materials and the new commercial products

Countries:
Sample Size: 50 per month, per year
Methodology: 20 minute online survey
Services Delivered: Recruitment

physicians and patients reported outcomes

Therapy Area: Haematology
Topic: beta-thalassemia
Respondent Type: Haematologists, haematologist-oncologists

+1

transfusion physicians

To obtain real-world evidence for patients with either transfusion-dependent beta-thalassemia or non-transfusion-dependent beta-thalassemia and specifically information on patients' demographic and clinical characteristics, treatment patterns, clinical outcomes, and health care resource utilization.

Countries:
Sample Size: 800 PRFs
Methodology: 75-minute pilots, 40-minute online survey (PRFs)
Services Delivered: Translations, recruitment, moderation and transcripts

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