New tapping therapy shows promise for trauma relief

NCT ID NCT07360990

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

43 people

The number who actually took part.

Started

Mar 2025

Finished

Jul 2025

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 to 65 years

Sex

Anyone

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

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

  • Zahide Betül Baydar

    Istanbul, Istanbul, 34876, Turkey (Türkiye)

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