Gentle craniosacral therapy tested to ease breast cancer After-Effects
NCT ID NCT04319510
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether craniosacral therapy, a gentle hands-on technique, can improve quality of life in women who have finished breast cancer treatment. 102 survivors with reduced well-being are randomly assigned to one-on-one therapy, group self-help training, or a waiting list. Researchers measure changes in cancer-related quality of life after 12 and 26 weeks.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- craniosacral therapy (a gentle hands-on technique)
- What this could lead to
- If it works, this could offer a safe, drug-free way to help breast cancer survivors feel better and improve their daily quality of life.
- What could go wrong
- This is a small, early-stage trial with no blinding, so results may be influenced by placebo effects. The therapy is complementary and not a treatment for cancer itself.
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
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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
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102 people
The number who actually took part.
- Started
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Sep 2023
- Finished
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Sep 2025
- Lead sponsor
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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
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Breast cancer (stage I-III) survivors after finishing curative chemotherapy and/or radiation * Impaired breast caner-related quality of life (\< 112,8 points on the FACT-B) Exclusion Criteria: * Planned surgery, adjuvant therapy (chemotherapy and/or radtiation), or rehabilitation during the study period * Pregnancy * Simultaneous participation in other clinical trials
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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
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Breast Unit, Evang. Kliniken Essen-Mitte
Essen, 45276, Germany
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Center for Integrative Medicine and Planetary Health, University Hospital Essen, University of Duisburg-Essen
Essen, 45130, Germany
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Department of Gynecology and Obstetrics, University Hospital Essen, University of Duisburg-Essen
Essen, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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