๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-07-13

Resolving Early Life Stress: Psychotherapy Outcomes and Neurobiology in Complex Depression (NCT07250893)

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿ“‹ Clinical Research Protocol Sponsor: St. Joseph's Healthcare Hamilton

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The RESPOND trial explores the link between early life adversity and later life depressive symptoms. The investigators have designed a new psychological therapy tailored to address the symptoms that can be caused by difficult experiences in early life. These symptoms include low mood, emotional dysregulation, and distressing thoughts and beliefs related to difficult or traumatic experiences. The investigators would like to see if this new therapy helps people feel better. The investigators are also studying the biological changes that can occur as a result of early life adversity, and how this therapy may influence those changes. To do this, the investigators ask questions about participants' physical and mental health and take blood samples.

Who can join: Review the eligibility criteria below.

Location: St. Joseph's Healthcare Hamilton โ€” Hamilton, Ontario

Age range: 18 Years to 65 Years

๐Ÿงช Interventions in This Study

  • Psychotherapy (OTHER)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (1 Sites)

  • St. Joseph's Healthcare Hamilton โ€” Hamilton, Ontario

๐Ÿ“ž Contact the Study Coordinator

Phone: (905) 522-1155

Email: dikaiosk@mcmaster.ca

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—