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RecruitingNCT05393492GREMO-LCAUpdated Jun 9, 2026

Regulating Emotions and Behaviors After Brain Injury

An interventional study of Dialectical Behavior Therapy and Radically Open dialectical behavior therapy in Acquired Brain Injury, Stroke/ Cerebrovascular Accident (Ischemic or Hemorrhagic) and Brain Tumor (After Recovery), sponsored by University Hospital, Strasbourg, France. Recruiting at 1 site in France. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-09.

Sponsored by University Hospital, Strasbourg, France · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started May 2022; still recruiting 4 years 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
77
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

After acquired brain injury (ABI), persons can experience emotional and behavioral difficulties, that can be painful both for the person and his/her family. This clinical study aims at measuring the effectiveness of a third wave cognitive behavioral therapy called "dialectical behavior therapy" (DBT). DBT aims at teaching persons emotion regulation skills, interpersonal effectiveness skills, mindfulness and distress tolerance skills through group and individual sessions.

The study's hypothesis is that DBT, in an adapted format for persons with ABI can lead to

  • a better quality of life, emotional and behavioral regulation, and self-esteem
  • decrease in problematic behaviors
  • progress in life goals
  • increase post traumatic growth and spirituality
  • better family functioning and lesser burden for care givers
  • experiencing more emotions and more free will

    45 persons with an ABI sustained more than 18 month back, will follow a 3 phases, follow-up with care as usual for 5 months, followed by 5 months of DBT, followed by 5 months of care as usual + DBT monthly sessions.

Self- and family-questionnaire will explore quality of life, emotional regulation, self-esteem, stress, anxiety, cognitive difficulties, family functioning and coping, post traumatic growth and spirituality and will be compared across the 3 phases. Results will be analyzed at a group level but also at an individual level (each patient separately) to test for decrease in unwanted behaviors and at a dyadic level (the person and his/her spouse) to test for the mutual effect of regulating emotions. Persons' memories will by analyzed at 3 time points by a linguistic analysis, and experience of free will after ABI will be analyzed by transcribed narratives of participants.

Read the detailed description

The study will explore the impact of Dialectical Behavior Therapy (DBT) skills training on patients with ABI, their families and on for their family system interactions.

->Triple methodology :

  1. 3 stages, monocentric, comparative, open-label for part of the outcome measures and single-blinded (only for linguistic markers) with active control treatment
  2. Prospective (at the individual level) and correlational (at the dyad level: client - family member) single-case experimental study exploring emotional-behavioral interactions as a function of the use of DBT skills by the client, over time.

    Further, it will explore the experience of free will (the property of the human will to determine itself freely), in relation to emotions and meaning of life/spirituality after ABI and the modifications of this experience after DBT.

  3. qualitative study of semi-structured individual by Interpretative Phenomenological Analysis (IPA

The objectives of this research are to show that a group training of DBT skills allows persons with ABI, (1) to improve quality of life - main objective; (2) to improve self-esteem and emotional regulation (3) to decrease depressive symptoms and problematic behaviors, (4) to self-determine and achieve one's goals (Goal Attainment Scaling) for a life worth living; (5) to improve coping and family functioning; (7) to decrease caregiver burden; (8) to interpret one's life, with more expression of emotions, non-judgment, acceptance of the difficulty of life and motivation to change (measured by linguistic analysis of emotionally charged memories)

02

Conditions studied

  • Acquired Brain Injury
  • Stroke/ Cerebrovascular Accident (Ischemic or Hemorrhagic)
  • Brain Tumor (After Recovery)
  • Encephalitis
  • Cerebral Anoxia
  • Meningitis

Keywords

  • brain injury
  • dialectical behavior therapy
  • emotions
  • emotional dysregulation
  • behavioral disorders
  • spirituality
  • challenging behaviors
  • linguistic markers
  • emotional distress
  • family burden
  • free will
  • interpretative phenomenological analysis
  • single-case experimental design
03

In context

Brain Injuries

946 studies on the registry are indexed under Brain Injuries; 235 are open to participants now.

This study's planned enrollment of 77 is above the median of 41 across 612 interventional studies indexed under Brain Injuries.

Browse Brain Injuries studies →

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 999 studies on the registry; 358 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Eligibility Criteria: * (Limit: 15,000 characters)

Summary criteria for participant selection.

Main eligibility criteria

GREMO patients :

  • Inclusion criteria:

    • Persons with acquired brain injury regardless of the type or location of the injury
    • Age between 18 and 68
    • Over 18 months since the acquired brain injury (or 6 month if mild traumatic brain injury)
    • Challenging behaviors or emotional dysregulation or high level of anxiety / depression or family's complaints about emotional dysregulation
    • Secondary or exacerbated by an acquired brain injury
    • Causing important suffering for themselves or their families
    • Being affiliated to a social security
    • Fluent in French
    • Being able to understand goals and risks and to give a dated and signed consent
  • Exclusion criteria:

    • Clinically evident severe lack of insight, lack of abstract reasoning, or severe anosognosia
    • Patients without any complaints
    • Severe cognitive impairments, aphasia or intellectual impairments that doesn't allow to understand DBT skills, questionnaires or group intreactions
    • Non fluent in French
    • Associated brain degenerative disease
    • Cancerous brain injury with uncertain progression
    • Non-stabilized psychotic disorder
    • Following a third wave cognitive behavioral therapy during the research study (for example : acceptance and commitment therapy)

Controls without brain injury

  • Inclusion criteria :

    • Being 18 years old or more
    • Without brain injury
  • Exclusion criteria :

    • Non fluent in French
    • History of brain injury or brain disease
    • History of psychiatric disorder
    • Personality disorder
    • GREMO patient's family member living together
    • Psychologist, neuropsychologist or people with an emotional regulation knowledge linked to their profession
    • Being under guardianship or curatorship
    • Being pregnant or breastfeeding

GREMO patients' family members

  • Inclusion criteria :

    • Being 18 years old or more
    • GREMO patient's family member
    • Living with a GREMO patient
    • Agreeing to rate an emotion-behavior-skills diary cards
  • Exclusion criteria :

    • GREMO patient's refusal for their family member to participate
    • Non fluent in French
    • Brain injury or brain disease
    • Major lack of insight
    • Being under trusteeship or curatorship

Qualitative research ABI patients and families

  • Inclusion criteria :

    • Person with ABI attending the same medico-social service as GREMO patients
    • Ineligible for GREMO patients group (participation refusal, major insight difficulty…)
    • Agreeing to talk about their free will or spirituality
  • Exclusion criteria :

    • Aphasia or dysarthria not allowing understandable recording
    • Impossibility to understand oral questions
    • Non fluent in French
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
77 participants (estimated)

Study arms

  • Experimental
    GREMO patients

    1. 5 months of baseline : usual care of in a medico-social service (medical, social, neuropsychological and psychological), 2. 5 months of dialectical behavior therapy (DBT) -DBT skills training group : during 19 weeks 3. 5 months of follow-up : usual care of + monthly reminders of DBT intervention skills

    Behavioral: Dialectical Behavior Therapy and Radically Open dialectical behavior therapy

  • No intervention
    Controls without brain injury

    People without brain injury used as controls for linguistic markers of emotional expression regulation and free will.

  • No intervention
    GREMO patients' family

    GREMO patients' relatives, without brain injury, living with the GREMO patient and ready to complete every day and adapted self-observational diary card similar to the one of the GREMO patient

  • No intervention
    Qualitative research ABI patients and families

    Patients and relatives followed by the same medico-social service but not meeting GREMO patients eligibility criteria, participating only in the qualitative research on free will and spirituality

Interventions

  • BehavioralDialectical Behavior Therapy and Radically Open dialectical behavior therapy

    Dialectical Behavior Therapy is a third wave cognitive-behavioral therapy. It focuses on emotional dysregulation and interactions between the patient and his family in genesis and maintenance of challenging behaviors. It is used here in an adapted form for cognitive problems. Delivered in a group format of 19 weeks + individual sessions.

06

What researchers measure

Primary outcomes

  1. Quality Of Life after Brain Injury

    Evaluation of quality of life after brain injury with QOLIBRI (Quality Of Life after Brain Injury)on 37 items belonging to 6 factors: cognition, self, daily life and autonomy, social relationships, emotions and physical problems. The Qolibri scores are reported a 0-100. 0 is the worst and 100 is the best. Self-rated by GREMO patients.

    Time frame: 15 months

Secondary outcomes

  1. Evaluation of the difficulties in emotions regulation

    Evaluation of emotional regulation difficulties with DERS ( Difficuties en Emotion Regulation Scale)-16 on 16 items filed in 5 factors : lack of emotional clarity, difficulties engaging in goal-directed behavior, impulse control difficulties, limited access to effective emotion regulation strategies, nonacceptance of emotional responses. Self-rated by GREMO patients and self-rated by family member about themselves. DERS-16 can range from 16 to 80, higher scores suggest greater problems with emotion regulation

    Time frame: 15 months

  2. Evaluation of self-esteem

    Evaluation of self-esteem on 10 items with EES-10 (Rosenberg Self-Esteem Scale) . You then get a score between 10 and 40.If you score below 25, your self-esteem is very low. Work in this area seems desirable. If you get a score above 39, your self-esteem is very high and you tend to be strongly assertive. Self-rated by GREMO patients

    Time frame: 15 months

  3. Evaluation of executive functioning

    Evaluation of executive functioning with BRIEF-A (Behavior Rating Inventory of Executive Function-Adult Version) on 75 items filed in inhibit, self-monitor, plan/organize, shift, initiate, task monitor, emotional control, working memory and organization of materials. Self-rated by GREMO patients and proxi-rated by a family member.high scores obtained on the BRIEF do not indicate a "disorder of executive function" but rather suggest a higher level of dysfunction in a specific domain of executive functions

    Time frame: 15 months

  4. Evaluation of reflective functioning

    Evaluation of reflective functioning with RFQ (Reflective Function Questionnaire) on 8 items. 7 if you strongly agree, and the 1 if you arestrongly disagree. Use the middle point (the 4) if you are neutral or indecisive requirements of the RFQ

    Time frame: 15 months

  5. Evaluation of psychological distress

    Evaluation of psychological distress with DASS-21 (Depression Anxiety Stress Scale) on 21 items about depression, anxiety and stress. Each of the 21 questions is scored on a 4-point scale ranging from 0 ("Did not apply to me at all") to 3 ("Applied to me very much, or most of the time"). Scores for Depression, Anxiety and Stress are calculated by summing the scores for the relevant items: Depression: 3, 5, 10, 13, 16, 17, 21 Anxiety: 2, 4, 7, 9, 15, 19, 20 Stress: 1, 6, 8, 11, 12, 14, 1

    Time frame: 15 months

  6. Evaluation of positive outcomes reported by persons who have experienced traumatic event

    Evaluation of positive outcomes reported by persons who have experienced traumatic events, such as brain injury, which evaluates new possibilities, relating to others, personal strength, spiritual change, and appreciation of life with Post-traumatic Growth Inventory. Self-rated by GREMO patients. It consists of 21 questions to which responses are given on a scale of 0-5, with 0 representing no change and 5 showing a great degree of change.

    Time frame: 15 months

  7. Evaluation of the perception of the family functioning

    Evaluation of the perception of the family functioning on 12 items with FAD (Family Assessment Device). Scores range from 1 to 4 with 1 reflecting healthy functioning and 4 reflecting unhealthy functioning.

    Time frame: 15 months

  8. Evaluation of coping cope with dysfunctions related to their relatives' pathology.

    Evaluation of coping cope with dysfunctions related to their relatives' pathology. Rated by a family member with FCQ (Family Coping Questionnaire).It consists of 21 questions to which responses are given on a scale of 0-5, with 0 representing no change and 5 showing a great degree of change.

    Time frame: 15 months

  9. Evaluation of family burden

    Evaluation of family burdenon 21 items with Zarit (Zarit Burden Interview) questionnaire Rated by a family member.The Zarit Burden Interview (ZBI) The ZBI consists of 22 items rated on a 5-point Likert scale that ranges from 0 (never) to 4 (nearly always) with the sum of scores ranging between 0-88. Higher scores indicate greater burden. A score of 17 or more was considered high burden

    Time frame: 15 months

  10. Evaluation of the goal attainment related to better emotional regulation

    3 milestone, 5-level GAS, evaluating goal attainment related to better emotional regulation. Each GREMO patient will have at least on personalized GAS according to his/her goals with Goal Attainment Scaling. 0 means not important, 1 means important, 2 means very important and 3 means extremely important

    Time frame: 15 months

07

Study locations

1 of 1 sites recruiting
  • Service EMOI-TC - Pôle de MPR Institut Universitaire de Réadaptation Clemenceau (IURC)
    Illkirch-Graffenstaden, 67402, France
    Recruiting
    • Agata KRASNY-PACINI · Contactagata.krasny-pacini@ugecam.assurance-maladie.fr · +33 3 69 06 30 42
    • Agata KRASNY-PACINI · Principal investigator
    • Marie-Eve ISNER-HOROBETI · Sub investigator
    • Maud ELBEL · Sub investigator
    • Guillaume BEHR · Sub investigator
    • Mathilde LAUGEL · Sub investigator
    • Marie KUPPELIN · Sub investigator
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05393492
Responsible party
Sponsor
First posted
May 26, 2022
Start date
May 19, 2022
Primary completion
May 19, 2022
Completion
Dec 2028 (estimated)
Last update
Jun 9, 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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