Clinical trial · Interventional
Supportive Effects of Craniosacral Therapy for Women With Breast Cancer
Supportive Effects of Craniosacral Therapy for Women With Breast Cancer: a Randomized Controlled Trial
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Craniosacral Therapy (CST) is a non-manipulative, very gentle, manual treatment method that aims to release restrictions of the fasciae and regulate the arousal of the sympathetic nervous system, which is often increased in chronically ill patients. Initial randomized trials support CST's efficacy and effectiveness in reducing symptoms of patients with psychosomatic and chronic pain disorders. To date, there is no trial investigating the effectiveness of CST as a supportive strategy for enhancing cancer-related quality of life in women with breast cancer. In clinical practice, therapists also report alleviating as well as regulating effects of simple CST self-help techniques, offered to patients within a group concept. Within the recent study, a CST treatment and self-help protocol for women after curative therapy of breast cancer was developed and shall be tested against a waiting list control group. The first group will receive 24 units of CST treatment in a 1:1 setting with a certified craniosacral therapist over 12 weeks. The second group will receive 24 units of group training in CST self-help techniques offered by a certified craniosacral therapist over 12 weeks. They will be reassessed after 12 and 26 weeks (6 months) after randomization. The third group will wait for 26 weeks and will receive no specific study intervention. After 26 weeks patients of the third group were offered self-selection to either individual CST or CST self-help group training. For all groups, treatment as usual is allowed.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Complementary Therapies | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Craniosacral self-help group training | Procedure | — | UNRESOLVED |
| Craniosacral therapy | Procedure | — | UNRESOLVED |
| Treatment as usal / wait list | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Craniosacral therapy
- description
- 24 CST units à 45 minutes over 12 weeks. Follow-up assessment 6 months after randomization.
- interventionNames
- Procedure: Craniosacral therapy
- type
- EXPERIMENTAL
- label
- Craniosacral self-help group training
- description
- 24 CST units à 45 minutes over 12 weeks. Follow-up assessment 6 months after randomization.
- interventionNames
- Procedure: Craniosacral self-help group training
- type
- OTHER
- label
- Treatment as usual / wait list control
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available