Blog

Case Studies: Telehealth, Fertility Preservation & Survivor Trials

Practical steps for running telehealth-enabled trials that integrate fertility preservation, safe vaccine studies in pregnancy, and breast cancer survivorship and family planning trials — with global regulatory checkpoints and actionable next steps.

Case Study: Caregiver-Inclusive MCI Trials & Survivor-Centered Gains

Analytical case study showing how caregiver-inclusive MCI trials and survivor-centered breast cancer endpoints—paired with decentralized visits and smarter logistics—reduce burden, boost retention, and reshape data management.

What if trials prioritized consent, sensory, caregiver & PRO needs?

Practical steps to make trials participant-centered: co-design consent, create sensory-friendly tinnitus BCI visits, embed caregiver workflows for breast cancer survivorship, and integrate PROs for MCI/PPA. Regulatory guidance supports this shift.

Case Study: Caregiver-Centered Consent Improves Breast Cancer Trials

Data-driven case study shows caregiver-centered consent, paired with remote symptom diaries and flexible visit models, boosts retention and improves breast cancer trial survivorship experience across diverse regulatory contexts.

Psilocybin Consent, Caregiver Protocols & Remote Monitoring: 7 Tips

{ "content": "When Mara's husband suffered a small stroke, the hospital team suggested a nearby post-stroke trial that used novel rehabilitation strategies and caregiver coaching. Mara's first question wasn't about protocol dates or compensation — it was, \"Will I know what to do if he has anxi...

Future Trials: Stroke Emotions, Aphasia Consent, Home GLP-1 & QoL

Analytical outlook on integrating emotional mapping for stroke, aphasia-friendly consent, home GLP-1 monitoring, and survivorship QoL — with comparative and cost-effectiveness analysis, plus a practical patient prep guide.

Expert Guide: Oncology Consent, Remote Monitoring & Survivorship Paths

Data-driven operational steps to improve oncology consent, reduce flu-season dropout via remote monitoring, and build breast cancer survivorship pathways—grounded in survey insights from clinicians and pharmaceutical project managers.

ClinConnect: Telehealth Consent Checklist & Oncology Burden Metrics

Data-driven analysis shows telehealth consent checklists reduce no-shows and that standardized burden metrics will reshape oncology trial design, with caregiver and working-parent logistics driving practical changes.

ClinConnect Report: eConsent, Stipends, Symptom-Tracking & Metabolic Trials

Practical guide to implement remote eConsent, stipend strategies, symptom-tracking templates, and recruitment tactics—step-by-step actions, diversity guidance, and a what-to-bring checklist.