Hypnosis may ease Chemotherapy's toll on breast cancer patients
NCT ID NCT04694885
First seen Jul 06, 2026 · Last updated Jul 07, 2026 · Updated 1 time
Summary
This study tests whether structured hypnotherapy sessions can improve quality of life for women with breast cancer undergoing chemotherapy. Participants in the intervention group receive 10 hypnotherapy sessions alongside standard care, while the control group receives standard care alone. Researchers will measure quality of life, side effects, anxiety, depression, and immune function. The goal is to see if adding hypnotherapy helps patients cope better during treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- structured hypnotherapy
- What this could lead to
- If it works, this could offer a drug-free way to help breast cancer patients feel better during chemotherapy, potentially becoming a standard part of cancer care.
- What could go wrong
- This is a small, early-stage study. The benefits may be modest or not statistically significant, and results may not apply to all breast cancer patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 62 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jul 2021
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Female participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Minimum Age 18 years * Female * Primary breast cancer * Receiving neo-adjuvant or adjuvant chemotherapy Exclusion Criteria: * Verbal or cognitive deficits that are not compatible with outpatient psychotherapy * Not consenting patients and vulnerable persons * Psychological disorders that prevent patients from participating in the study (e.g. psychotic disorder) * acute suicidality
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Breast cancer are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University Hospital Basel
Basel, Canton of Basel-City, 4056, Switzerland
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a common steroid shield breast cancer patients from a dangerous drug side effect?
- Tiny magnetic seeds could guide surgeons to the right lymph node
- Can a tiny clip spare breast cancer patients full lymph node removal?
- New PET tracer aims to light up hidden cancer targets
- Gut bacteria supplement tested against chemo hair loss
- Can a mindfulness program boost Self-Compassion in breast cancer survivors?