- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05393492
Regulating Emotions and Behaviors After Brain Injury (GREMO-LCA)
Dialectical Behavior Therapy for Challenging Behaviors and Emotional Distress After Acquired Brain Injury : a Pilot Study
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.
Study Overview
Status
Conditions
Intervention / Treatment
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 :
- 3 stages, monocentric, comparative, open-label for part of the outcome measures and single-blinded (only for linguistic markers) with active control treatment
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.
- 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)
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Illkirch-Graffenstaden, France, 67402
- Recruiting
- Service EMOI-TC - Pôle de MPR Institut Universitaire de Réadaptation Clemenceau (IURC)
-
Contact:
- Agata KRASNY-PACINI
- Phone Number: +33 3 69 06 30 42
- Email: agata.krasny-pacini@ugecam.assurance-maladie.fr
-
Principal Investigator:
- Agata KRASNY-PACINI
-
Sub-Investigator:
- Marie-Eve ISNER-HOROBETI
-
Sub-Investigator:
- Maud ELBEL
-
Sub-Investigator:
- Guillaume BEHR
-
Sub-Investigator:
- Mathilde LAUGEL
-
Sub-Investigator:
- Marie KUPPELIN
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: GREMO patients
|
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. |
|
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
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality Of Life after Brain Injury
Time Frame: 15 months
|
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. |
15 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of the difficulties in emotions regulation
Time Frame: 15 months
|
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 |
15 months
|
|
Evaluation of self-esteem
Time Frame: 15 months
|
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 |
15 months
|
|
Evaluation of executive functioning
Time Frame: 15 months
|
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 |
15 months
|
|
Evaluation of reflective functioning
Time Frame: 15 months
|
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 |
15 months
|
|
Evaluation of psychological distress
Time Frame: 15 months
|
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 |
15 months
|
|
Evaluation of positive outcomes reported by persons who have experienced traumatic event
Time Frame: 15 months
|
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. |
15 months
|
|
Evaluation of the perception of the family functioning
Time Frame: 15 months
|
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.
|
15 months
|
|
Evaluation of coping cope with dysfunctions related to their relatives' pathology.
Time Frame: 15 months
|
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. |
15 months
|
|
Evaluation of family burden
Time Frame: 15 months
|
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 |
15 months
|
|
Evaluation of the goal attainment related to better emotional regulation
Time Frame: 15 months
|
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 |
15 months
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Neuroinflammatory Diseases
- Cerebrovascular Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Vascular Diseases
- Cardiovascular Diseases
- Wounds and Injuries
- Pathologic Processes
- Neoplasms by Site
- Neoplasms
- Signs and Symptoms, Respiratory
- Nervous System Neoplasms
- Craniocerebral Trauma
- Trauma, Nervous System
- Central Nervous System Neoplasms
- Hypoxia
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Stroke
- Ischemia
- Mental Disorders
- Brain Injuries
- Brain Neoplasms
- Meningitis
- Encephalitis
- Hypoxia, Brain
- Behavior Therapy
- Psychotherapy
- Behavioral Disciplines and Activities
- Dialectical Behavior Therapy
Other Study ID Numbers
- 8264 (CTEP)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Encephalitis
-
National Institute of Allergy and Infectious Diseases...CompletedAlphavirus Infections | Eastern Equine Encephalitis | Venezuelan Equine Encephalitis | Western Equine EncephalitisUnited States
-
Medical University of ViennaAustrian Science Fund (FWF)CompletedTick Borne EncephalitisAustria
-
PfizerCompletedTick-borne Encephalitis (TBE)Poland
-
PATHCompletedEncephalitis, Japanese BPhilippines
-
Medical University of ViennaValneva Austria GmbHUnknownImmune Responses After a Booster Immunisation With IXIARO® in Elderly Compared to Young Individuals.Japanese Encephalitis VaccineAustria
-
Indian Institute of ScienceWellcome Trust; PATH; University of Liverpool; National Institute of Mental Health...CompletedJapanese Encephalitis | Japanese Encephalitis VaccineIndia
-
Mahidol UniversityCompletedEncephalitis, Japanese BThailand
-
Valneva Austria GmbHCompleted
-
Valneva Austria GmbHCompletedEncephalitisUnited States, Australia, Denmark, Germany, Sweden
-
National Institute of Hygiene and Epidemiology,...Ministry of Health, Vietnam; Ministry of Science and Technology, VietnamCompleted
Clinical Trials on Dialectical Behavior Therapy and Radically Open dialectical behavior therapy
-
Uppsala University HospitalThe Söderströmska-Königska Foundation; Fonden för psykisk hälsa; Forskningsrådet...RecruitingAnorexia Nervosa | Feeding and Eating Disorders | Eating Disorders | Anorexia Nervosa, AtypicalSweden
-
Washington University School of MedicineCompletedAnorexia Nervosa | Obsessive-Compulsive Disorder | Social Phobia | Depression, AnxietyUnited States
-
University of WindsorRecruitingDepression | Mood Disorders | Stress | Anxiety | Depression - Major Depressive DisorderCanada
-
University Hospital, Strasbourg, FranceCompletedAutism Spectrum DisordersFrance
-
Pontificia Universidad Catolica de ChileUniversity Diego PortalesNot yet recruitingBorderline Personality DisorderChile
-
University of WashingtonNational Institute of Mental Health (NIMH)CompletedSuicide | Post-traumatic Stress Disorder | Self-injurious BehaviorUnited States
-
Umeå UniversityActive, not recruitingAnorexia Nervosa | Anorexia in Adolescence | Anorexia Nervosa, AtypicalSweden
-
Fordham UniversityNot yet recruitingAntisocial Personality DisorderUnited States
-
Rutgers, The State University of New JerseyCompletedBorderline Personality DisorderUnited States
-
Masarykova UniverzitaBrno University Hospital; Masaryk UniversityCompletedBorderline Personality DisorderCzech Republic