CompletedNot Applicable

Psychological Interventions to Prevent Late Effects in Breast Cancer

Norway203 participantsStarted 2020-10-01

Plain-language summary

The study aims to investigate whether a combined pre-operative medical hypnosis plus a post-operative internet-based acceptance and commitment intervention are more effective in preventing post-surgical pain and fatigue following breast cancer surgery compared with pre-operative mindfulness plus treatment as usual.

Who can participate

Age range18 Years – 70 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Women diagnosed with breast cancer and scheduled for surgery * Be able to provide informed consent Exclusion Criteria: * Insufficient Norwegian speaking or writing skills to participate in the interventions and fill out questionnaires * Cognitive and psychiatric impairment * Other serious malignancies

What they're measuring

Chronic post-surgical pain

Timeframe: 3 months after surgery

Post-surgical fatigue

Timeframe: 3 months after surgery

Trial details

NCT IDNCT04518085

SponsorUniversity of Oslo

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-03-03

View on ClinicalTrials.gov More Pain, Postoperative trials