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Pre-operative Hypnosis to Prevent Side Effects After Surgery

NCT04300283 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2021-06-09

No results posted yet for this study

Summary

The aim of the pilot study is to translate and feasibility test a brief hypnosis intervention in 8-10 patients that are about to undergo thoracic surgery and in 4-5 patients about to undergo breast cancer surgery.

Conditions

  • Breast Cancer Surgery

Interventions

BEHAVIORAL

Hypnosis

See previous description

Sponsors & Collaborators

  • Oslo University Hospital

    lead OTHER

Principal Investigators

  • Silje E Reme, PhD · Oslo University Hospital

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-01
Primary Completion
2020-12-31
Completion
2020-12-31

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04300283 on ClinicalTrials.gov