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RecruitingNCT07342270SPiPSUpdated Oct 16, 2026

Sensorimotor Psychotherapy for Personality Disorders

An interventional study of Sensorimotor Psychotherapy and Treatment as ususal in Early Chilhood Trauma and Personality Disorder, sponsored by Tilburg University. Recruiting at 6 sites in Netherlands. Open to participants aged 16 Years and older. Per ClinicalTrials.gov, last updated 2026-10-16.

Sponsored by Tilburg University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started May 2026; still recruiting 6 months later.
Updated Oct 16, 2026Now RecruitingFirst site in Netherlands+3 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
131
Allocation
Randomized
Ages
16 Years and older
Sex
All
01

Study summary

SUMMARY

Rationale: Personality disorders are treated conform the Dutch GGZ-zorgstandaard mainly with verbal psychotherapies but experts by experience call out to make use of body-oriented approaches as well. In general, the rationale to study the effects of bodily centered therapy for personality disorders is built on the overlap between personality disorders and posttraumatic stress disorder (PTSD). In both classifications, childhood major events and/or traumatic life events play a role in the history of its origins (Karatzias et al., 2023).Traditional psychotherapies for personality disorders address the cognitive and emotional elements of trauma, but lack techniques that work directly with the physiological elements, although trauma profoundly affects the body and many symptoms of traumatized individuals with personality disorders are somatically based. However, studies into the effect of body centered interventions for personality disorders are scarce. This study aims to examine the effects of sensorimotor psychotherapy (SP), a body-oriented intervention, in patients with a personality disorder and PTSD-symptoms. This study studies the effect of sensorimotor psychotherapy (SP) which is a body-oriented intervention which focuses on the combination of a personality disorder and post-traumatic stress disorder.

Objective: This multi-center randomized controlled study aims to research the effect of a 12-session sensorimotor psychotherapy (SP) group intervention, in comparison with treatment-as-usual, on emotion regulation in people with a personality disorder. In addition, the effects on body awareness, self-soothing, PTSD-symptoms and personality functioning are assessed. Patients' perception of the intervention will be assessed through qualitative techniques. The study will be carried out in five mental health institutions in the Netherlands.

Study design: This is a multi-center randomized controlled trial, in which the intervention group receives a 12-sessions SP-therapy, and the control group receives treatment-as-usual of the assigned institution. Measurements through standardized instruments take place at three moments: pre-intervention (T0), post-intervention (T1), and two months follow-up (T2). Qualitative interviews are conducted after completion of the SP-condition. In combination with the qualitative measurements, a Mixed Methods Design is used.

Study population: Patients older than 18 years, who have been diagnosed with a personality disorder and have experienced early childhood trauma.

Intervention: patients assigned to the SP-condition receive the 12-session SP group protocol (Fisher \& Ogden, 2016), this protocol introduces diverse successive skills, aiming for the patient to have more somatic resources to regulate arousal of the autonomous nervous system. Every session starts with psychoeducation on a trauma-related theme, followed by one or multiple skills which are practiced in dyads and are later discussed in the group. The subjects which are covered are: autonomous arousal, implicit memory, regulation techniques, survival sources, somatic and internal resources, boundaries, practicing with experiments and repetitions, focus on positive change.

Main study parameter: The main parameter of this study is emotion regulation. Emotion regulation is examined with the Difficulties in Emotion Regulation Scale - Short Form (DERS-SF).

Secondary parameters: Second parameters are body awareness, self-soothing, PTSD-symptoms, personality functioning. Body awareness is examined with the Multidimensional Assessment of Interoceptive Awareness (MAIA-2). The Soothing Receptivity Scale (SRS) is used to examine self-soothing abilities. The PTSD-checklist for DSM-5 (PCL-5) is used to assess the PTSD-symptoms. The Level of Personality Functioning Scale-Brief Form 2.0 (LPFS-BF 2.0) is used to map out personality functioning. The patients' perception of the intervention is explored through qualitative interviews. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients involved in this study are indicated for treatment for a personality disorder. Sensorimotor psychotherapy belongs the treatment options of some mental health institutions. Additionally, patients who are assigned to the control condition are offered the SP-condition after completing the control condition. In this way they can also benefit from the SP-condition.

Questionnaires are filled in at three moments during the treatment (T0, T1, T2), filling in the questionnaires will take 60 minutes on average, which is little more than routine outcome measurement takes in Dutch mental healthcare. The qualitative interviews after the SP-condition will take up 60 minutes on average.

02

Conditions studied

  • Early Chilhood Trauma
  • Personality Disorder

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Keywords

  • Sensorimotor Psychotherapy
  • Personality disorders
  • Early childhood trauma
  • SP-protocol
03

In context

Personality Disorders

126 studies on the registry are indexed under Personality Disorders; 24 are open to participants now.

This study's planned enrollment of 131 is above the median of 84 across 81 interventional studies indexed under Personality Disorders.

Browse Personality Disorders studies →

Lead sponsor

Tilburg University is the lead sponsor of 27 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Aged 16 and older
  • Diagnosed with a personality disorder according to the DSM-classification
  • Has a history of early childhood trauma

Exclusion criteria

Exclusion Criteria:

  • Does not master Dutch / English sufficiently for filling out the questionnaire cannot fill participate in the research.
  • Presents factors or behaviour that disrupts participation in the group and undermines treatment will be excluded from this study.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
131 participants (estimated)

Study arms

  • Active comparator
    Treatment as usual

    Treatment as usual for personality disoders

    Other: Treatment as ususal

  • Experimental
    Sensorimotor Psychotherapy

    Sensorimotor Psychotherapy 12-session group protocol

    Other: Sensorimotor Psychotherapy

Interventions

  • OtherSensorimotor Psychotherapy

    Sensorimotor psychotherapy (SP) is a body-oriented approach for people with personality disorders. The SP-intervention consists of 12-session SP-protocol which is applied in a groupsetting. Each session starts with psycho-education on a trauma-related topic, followed by one or multiple skills which are practized and discussed within the group.

  • OtherTreatment as ususal

    The control condition consists of the standard treatment for personality disorders as provided within the mental health care institution. This treatment may comprise various components, depending on the specific institution. The nature and extent of the treatment provided will be documented.

06

What researchers measure

Primary outcomes

  1. Emotion regulation-Difficulties in Emotion Regulation Scale

    The Difficulties in Emotion Regulation Scale (DERS) is used to assess the primary parameter, emotion regulation (Kaufman et al., 2016). This is a 36 item self-report questionnaire for evaluating emotion regulation problems. The factors correspond to the six factors from the scale. The scales are: 1. not accepting emotional responses, 2. difficulties in showing goal-directed behavior, 3. problems with impulse control, 4. lack of emotional awareness, 5. limited access to emotion regulation strategies, and 6. lack of emotional clarity. The questionnaire has excellent validity and reliability (Cronbach's alpha = 0.89) (Kaufman et al., 2016). A higher score indicates more problems in emotion regulation.

    Time frame: A pre-intervention, post-intervention and follow-up (8-weeks post-intervention).

Secondary outcomes

  1. Body awareness- Multidimensional Assessment of Interoceptive Awareness

    Multidimensional Assessment of Interoceptive Awareness (MAIA-2) (Mehling et al., 2018) is used to assess the extent of body awareness. This is a 37-item self-report questionnaire with a 6-point Likert scale focusing on interoceptive awareness. There are 8 subscales: noticing, not-distracting, not-overthinking, attention regulation, emotional awareness, self-regulation, body awareness and confidence. Cronbach's alpha varies from 0.67 to 0.89 on the subscales and factor structure is confirmed (Mehling et al., 2015; Scheffers et al., 2024). A higher score indicates more body awareness.

    Time frame: A pre-intervention, post-intervention and follow-up (8-weeks post-intervention).

  2. Self-soothing-Soothing Receptivity Scale

    Soothing Receptivity Scale (SRS) (Glassman, 1988) is used to assess receptivity to calm. This is a 27-item self-report questionnaire with a 5-point Likert scale to assess the experience being calmed down, being physically calmed down, the experience of calming down by sharing emotions with others and self-soothing. The SRS has good internal consistency (Cronbach's alpha = 0,80). The higher the score, the more capable one is to self-sooth.

    Time frame: A pre-intervention, post-intervention and follow-up (8-weeks post-intervention).

  3. PTSD-symptoms - PTSD-checklist for DSM-5

    PTSD-checklist for DSM-5 (PCL-5) is a 20-item self-report questionnaire which questions symptoms of PTSD on a 5-point Likert Scale with a good reliability (Cronbach's alpha =0.94), test-retest reliability and discriminating validity (Blevins et al., 2015). A change of 5 points is seen as a relevant change during treatment. A change of 10 points in total score is a minimum for clinical relevant changes.

    Time frame: A pre-intervention, post-intervention and follow-up (8-weeks post-intervention).

  4. Level of Personality functioning - Level of Personality Functioning Scale-Brief Form 2.0

    Level of Personality Functioning Scale-Brief Form 2.0 (LPFS-BF 2.0) (Weekers et al.,2019) assesses personality functioning. The LPFS-BF is a 12-item self-report questionnaire with a 4-point Likert Scale and gives the general severity of the personality pathology based on the Alternative Model for Personality disorder from section III of the DSM-5. The items are clustered in two higher domains, Self-functioning and Interpersonal functioning. The questionnaire is sufficient reliability and is sensitive for change. A score higher than 2 on one of the two domains refers to problems in personality functioning. A higher score indicates more disfunctioning.

    Time frame: A pre-intervention, post-intervention and follow-up (8-weeks post-intervention).

07

Study locations

6 of 6 sites recruiting
  • GGz Centraal Fornhese
    Ermelo, Gelderland 3850BA, Netherlands
    Recruiting
  • GGNet Scelta
    Warnsveld, Gelderland 7231PA, Netherlands
    Recruiting
  • enMente
    Zutphen, Gelderland 7201AL, Netherlands
    Recruiting
  • GGz Breburg
    Tilburg, North Brabant 5025JE, Netherlands
    Recruiting
  • Aelbrecht GGz
    Waalre, North Brabant 5582LA, Netherlands
    Recruiting
  • Topp-Zorg
    Zeist, Utrecht 3705LZ, Netherlands
    Recruiting
08

Updates

1 registry update since Sep 25, 2026
Status
Not yet recruiting→Recruiting
changed Oct 16, 2026
Sites
6 sites added — first site in Netherlands
Show 6 added (6 Netherlands)
  • GGz Centraal Fornhese · Ermelo, Netherlands
  • GGNet Scelta · Warnsveld, Netherlands
  • enMente · Zutphen, Netherlands
  • GGz Breburg · Tilburg, Netherlands
  • Aelbrecht GGz · Waalre, Netherlands
  • Topp-Zorg · Zeist, Netherlands
Oct 16, 2026
Start date
Feb 1, 2026→May 1, 2026 (actual)
Oct 16, 2026
Primary completion
Feb 1, 2028→May 1, 2028
Oct 16, 2026
Show all 1 update
  1. Oct 16, 2026
    Not yet recruiting→Recruiting
    6 sites added — first site in Netherlands
    Show 6 added (6 Netherlands)
    • GGz Centraal Fornhese · Ermelo, Netherlands
    • GGNet Scelta · Warnsveld, Netherlands
    • enMente · Zutphen, Netherlands
    • GGz Breburg · Tilburg, Netherlands
    • Aelbrecht GGz · Waalre, Netherlands
    • Topp-Zorg · Zeist, Netherlands
    Start date Feb 1, 2026→May 1, 2026 (now actual)
    Primary completion Feb 1, 2028→May 1, 2028
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07342270
Lead sponsor
Tilburg University
Collaborators
GGZ Breburg
Responsible party
Sponsor
First posted
Jan 15, 2026
Start date
May 1, 2026
Primary completion
May 1, 2028 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Oct 16, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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