Self-Hypnosis for the Enhanced Recovery after Surgery in Patients with Gynecologic Cancer
- Undergoing an exploratory laparotomy for suspected gynecologic cancer, which includes metastatic disease from neoplasia originating in other organs
- Planned participation in the Gynecologic Enhanced Recovery Pathway
- Patient must be able to read, understand, and speak English
- Consents to being part of a randomized study
- Patient has physical and mental capabilities to take part in study
- Sensitivity to amide-type local anesthetics
- Patients on long-acting opioid medications, or scheduled (four or more times a day for seven or more days) short-acting opioid medications within the last 30 days
- Emergency surgery of any type that does not allow for proper time for protocol review by the patient
- Surgery that involves known/anticipated resection of anterior abdominal wall with plastic surgery reconstruction
- Patients undergoing known/anticipated anterior abdominal wall hernia repairs
- Patients undergoing pelvic exenteration
- Patients with known major psychiatric disease
- Patients with hearing impairment such that they are unable to hear the intervention
I. To evaluate whether participation in pre-operative self-hypnosis (SH) is feasible and will improve patients' perception of post-surgical pain, after undergoing open gynecologic surgery (laparotomy) on an enhanced recovery pathway.
I. To evaluate whether participation in pre-operative SH is associated with changes in use of opioid medication, including time to first postoperative opioid and total dose of opioids taken (converted to morphine equivalents) and avoidance of opioids.
II. To explore whether participation in pre-operative SH is associated with changes in length of stay.
III. To explore whether there are differences between the two study arms in other common symptoms of women undergoing gynecologic surgery, functional recovery after surgery and quality of life (QOL).
IV. To explore whether expectations regarding symptom management or hypnotic susceptibility are related to or influence the perception of symptoms after surgery.
V. To measure satisfaction with the intervention (patients on arm 2).
VI. To perform sub analyses to explore whether other common clinical or demographic factors are potential covariates.
I. To compare two different instruments measuring patient reported outcomes in hospital postoperative recovery.
OUTLINE: Patients are randomized to 1 of 2 arms.
ARM I: Patients receive usual care including receipt of multi-modal analgesia and the injection of a local analgesic at the time of surgery on the enhanced recovery after surgery (ERAS) pathway.
ARM II: Patients receive usual care as in Arm I. Patients also receive self-hypnosis guided relaxation by listening to MP3 on the ERAS pathway.
Trial Phase Phase NA
Trial Type Supportive care
M D Anderson Cancer Center
Larissa Alejandra Meyer
- Primary ID 2018-0143
- Secondary IDs NCI-2019-08222
- Clinicaltrials.gov ID NCT04266886