New tapping therapy shows promise for trauma relief
NCT ID NCT07360990
First seen Jun 27, 2026 · Last updated Jul 15, 2026 · Updated 2 times
Summary
This pilot study tested a new therapy called Psychological Cognitive Reprocessing Procedure (P-CRP) in 43 adults with trauma and grief. Unlike standard treatments, P-CRP starts by silently repeating a word tied to a negative belief while tapping the shoulders, letting the mind process memories on its own. The study compared P-CRP to an active control and a waitlist, measuring changes in trauma symptoms and anxiety.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Psychological Cognitive Reprocessing Procedure (P-CRP) - a behavioral therapy using silent repetition of a negative belief word with bilateral tapping
- What this could lead to
- If this therapy works, it could offer a new way to reduce trauma and grief symptoms without directly confronting traumatic memories.
- What could go wrong
- This is a very small pilot study (43 people) with no phase, so results may not apply broadly. The therapy is new and unproven, and the study is completed but not yet published in a peer-reviewed journal.
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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43 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Jul 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 to 65 years
- Sex
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Anyone
- 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.
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.
Individuals were excluded if they had: 1. An Adverse Childhood Experiences (ACE) score greater than 7. 2. A history of psychotic disorder or bipolar disorder. 3. Current suicide risk. 4. Substance use disorder. 5. Prior therapeutic contact with the researcher. 6. A target traumatic event that had occurred more than one year earlier. 7. Not meeting clinical DSM-5 criteria for PTSD during the clinician-administered semi-structured interview, regardless of initial self-report scores. 8. Current participation in any other form of psychotherapy or psychiatric intervention. Individuals were included if they had: 1. Meeting DSM-5 criteria for PTSD symptoms (verified by IES-R scores and clinician-led semi-structured interview). 2. Having experienced a target traumatic event or loss within the past 12 months. 3. Willingness to provide informed consent and participate in all intervention sessions.
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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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Zahide Betül Baydar
Istanbul, Istanbul, 34876, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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