๐๏ธ Verified NIH Record โข Updated 2026-07-22
REmotely-delivered Supportive Programs for Improving Surgical Pain and disTrEss (NCT05625360)
REmotely-delivered Supportive Programs for Improving Surgical Pain Dnd disTrEss (RESPITE)
๐ต Active, Not Recruiting Phase3 ๐ Clinical Research Protocol Sponsor: Wake Forest University Health Sciences
๐ฉบ Plain-English Summary (8th-Grade Level)
The purpose of this research study is to learn how two different supportive programs may help women feel better after surgery. This study will measure if one type of supportive program is more useful than the other for improving wellbeing after surgery.
Who can join: Review the eligibility criteria below.
Location: Atrium Health - Levine Cancer Institute โ Charlotte, North Carolina
Age range: 18 Years
๐งช Interventions in This Study
- eHealth Mindful Movement and Breathing (OTHER)
- Life Impacts Reflection (OTHER)
- PROMIS Questionnaires (OTHER)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (2 Sites)
- Atrium Health - Levine Cancer Institute โ Charlotte, North Carolina
- Wake Forest Baptist Comprehensive Cancer Center โ Winston-Salem, North Carolina
๐ฐ 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.
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Explore by condition: All Postoperative Pain, Acute clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.