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December 13th, 2024

Exploring Clinical Trials: Debunking Myths and What to Know

This conversation focuses on the significance of clinical trials in the context of Parkinson’s disease, featuring insights from Stephanie Farrell, Director of Research Administration at Eisenhower Health. The discussion covers the importance of clinical trials, the different types and phases of research, the informed consent process, and the risks and benefits of participation. It also addresses common myths about clinical trials, the patient experience, and the costs associated with participation. The conversation emphasizes the need for patient advocacy and the importance of understanding disease progression alongside potential treatments.

Chapters
00:00 | Introduction to Clinical Trials and Research
03:11 | Importance of Clinical Trials
05:46 | Types of Clinical Research
07:48 | Phases of Clinical Trials
11:31 | Risks and Benefits of Participation
16:20 | Informed Consent Process
19:53 | Myths and Misconceptions about Clinical Trials
22:43 | Randomization in Clinical Trials
26:05 | Patient Experience in Clinical Trials
31:11 | Making Informed Treatment Decisions
36:18 | Costs Associated with Clinical Trials
39:47 | Encouraging Local Clinical Trials
49:53 | Importance of Understanding Disease Progression

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Need help finding resources for you or your loved one after being diagnosed with Parkinson’s? Check out our Wellness Village Resource Directory using the link:
www.parkinsonsresource.org/the-wellness-village

Click the link to see our Support Groups and Village Meetings. www.parkinsonsresource.org/news/calendar/

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Instagram: https://www.instagram.com/parkinsonsresourceorg/

Contact us!
Address | Parkinson’s Resource Organization
74785 Highway 111 Suite 208
Indian Wells, CA 92210

Toll-Free Phone | (877) 775-4111

Email | info@parkinsonsresource.org

Parkinson’s Resource Organization, working so no one is isolated because of Parkinson’s

Jo Rosen Founder & President of Parkinson’s Resource Organization

Jo is the founder and President of Parkinson’s Resource Organization (PRO) established in 1990. The motivation, her late mother and late husband were both diagnosed with Parkinson’s. Each day, PRO reaches thousands of people affected by Parkinson’s, accomplished through a monthly newsletter, an interactive website, one-on-one coaching, support groups, symposia, and public speaking. Ms. Rosen is always at the forefront of what matters in Parkinson’s from services, products, and research, to the potential cure.

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