Gentle touch for aching knees: craniosacral therapy tested in new study
NCT ID NCT07372534
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether adding craniosacral therapy (a gentle, hands-on technique) to a home exercise program could reduce pain and improve function in people with knee osteoarthritis. Twenty-one adults participated, with one group receiving the therapy weekly for six weeks plus exercises, and the other doing exercises alone. Researchers measured pain, heart rate variability, stiffness, and quality of life before and after treatment.
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
- What this could lead to
- If it works, this could offer a gentle, hands-on option to help manage knee osteoarthritis pain and stiffness without drugs.
- What could go wrong
- This is a very small, early-stage trial with only 21 participants. Results may not apply to everyone, and the therapy's benefits are uncertain.
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
-
21 people
The number who actually took part.
- Started
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Apr 2023
- Finished
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Mar 2024
- 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
-
40 to 85 years
- Sex
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Anyone
- Healthy volunteers
-
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: * Age between forty and eighty-five years * Diagnosis of knee osteoarthritis * Ability to understand the study procedures and provision of written informed consent Exclusion Criteria: * Consumption of caffeine within the last four hours or use of tobacco within the last forty-eight hours prior to assessment * Use of alcohol or recreational drugs within the last week * Eating within two hours before the assessment * History of neuropathic disorders * History of unexplained syncope episodes * Inability to move independently * Presence of uncontrolled medical conditions, such as cardiac (e.g., angina) or respiratory (e.g., asthma) diseases * Presence of neurological disorders, including Parkinson's disease or multiple sclerosis * History of vascular surgery or open knee surgery, or receipt of a knee injection within the last one month * Presence of somatic dysfunction symptoms or musculoskeletal injuries that may interfere with assessments * Diagnosis of pregnancy, sarcopenia, cognitive impairment, or osteoporosis * Any medical condition affecting the autonomic nervous system or immune system, including autonomic neuropathy, pure autonomic failure, autoimmune diseases, or acquired immunodeficiency syndrome
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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
-
Ankara Yıldırım Beyazıt University
Ankara, 06010, Turkey (Türkiye)
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