- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05534763
Internet-delivered Treatment for Transgender Individuals With Co-occurring Mental Health Problems (IERGD)
Internet-delivered Emotion Regulation Treatment (I-ER GD) for Transgender Adults and Co-occurring Mental Health Problems
This project aims to develop and evaluate if an internet delivered psychological intervention for transgender individuals undergoing assessment for gender dysphoria and a support person, is feasible, acceptable and effective in increasing emotional skills, strengthening a healthy identity development, social support and resilience to current and future mental illness.
In two studies, a psychological treatment for transgender adults (18+) seeking health care for gender dysphoria and a support person (i.e., relative, friend) will be evaluated.
The project will be carried out at a specialized unit for transgender health care (ANOVA) at Karolinska University Hospital
Study Overview
Status
Intervention / Treatment
Detailed Description
There are no psychosocial treatments for young transgender adults seeking treatment for gender dysphoria - psychological distress due to the incongruence between one's assigned sex and one's gender identity. This project aims to develop and evaluate if an internet delivered psychological intervention for individuals undergoing assessment for gender dysphoria and a support person, is feasible, acceptable and effective in increasing emotional skills, strengthening a healthy identity development, social support and resilience to current and future mental illness.
Data and Method: In three studies, a psychological treatment for transgender adults (18+) seeking care for gender dysphoria and a support person (i.e., relative, friend) will be evaluated. Study 1 is a feasibility study (N=40) with pre-, post- and weekly assessments evaluating the intervention's feasibility, credibility, acceptability and preliminary efficacy. Study 2 is a qualitative interview study exploring participants' experience of the intervention.
Plan for project realization: The project will be carried out at a specialized unit for transgender health care (ANOVA) at Karolinska University Hospital, with a large patient recruitment base and extensive experience of clinical studies providing good opportunities for later implementation in regular care.
Relevance: Studies show elevated rates of psychopathology in transgender adults. It has been suggested that experiences of minority stress, e.g., discrimination, internalized transphobia and gender identity concealment exhausts the ability to regulate negative emotions in an adaptive way. There is a need for treatment and preventive psychological interventions, particularly as the number of young transgender adults seeking gender affirming treatment has increased markedly during the 2000s. This project will lead to increased knowledge about the specific needs of this growing patient group and develop health care in accordance with national guidelines.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Stockholm, Sweden, 17176
- ANOVA, Karolinska University Hospital, Norra Stationsgatan 69, Plan 4
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients having had an initial assessment at ANOVA for GD between March 2022 and November 2022 and found eligible for a diagnostic assessment period and having been put on a waitlist for continued evaluation.
- Being at least 18 years of age;
- Reporting elevated self-perceived psychiatric symptoms (e.g., depression, anxiety, suicidality) or functional impairment (difficulties maintaining school, work or daily routines);
- Be able to write and read in Swedish; and
- Have daily access to a computer with internet connection.
Exclusion Criteria:
- Evidence of active untreated mania, psychosis or other severe psychiatric symptoms that are deemed primary and need treatment;
- Current and increased suicide risk, such as intrusive suicide thoughts, or current suicide plans, or recent suicide attempt;
- Current enrollment in another psychological intervention study or currently receiving regular psychological treatment or
- Less than 6 weeks of stable psychopharmacotherapy if such treatment is ongoing.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: IERGD
I-ER GD is a 10-week intervention directed to the person with GD, provided via the internet with therapist-support.
During treatment, participants have an assigned psychologist to interact with and be offered support by, either through feedback on assignments, asynchronous chats or, if needed, by telephone.
I-ER GD will focus on increasing adaptive emotion regulation skills, healthy identity development, interpersonal effectiveness skills, coping and building a resilient lifestyle through psychoeducation on gender minority stress, practicing adaptive emotion regulation skills, and reducing emotional and behavioral avoidance.
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A 10 week behavioral treatment focusing on gender minority stress, maladaptive and adaptive emotion regulation, emotional awareness, the functionality of emotions, interpersonal skills and values and valued actions.
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|
Other: IER SUPPORT
I-ER Support is a 5-week intervention directed to a support person, provided as an optional addition to I-ER GD.
I-ER Support is administered in the same manner and in parallel to the I-ER GD intervention.
Treatment content is based on the same principles as I-ER GD, but from the perspective of increasing emotional support and understanding of GD.
The support person could benefit from increased coping and emotion regulation skills, as they may also be exposed to discrimination or stigma due to having a transgender child, sibling or loved one.
In better understanding the processes of being stigmatized and with improved emotion regulation skills, the support person may offer better support and help alleviate burdening effects for the individual with GD.
For this reason, I-ER support is primarily aimed at people without trans-experience.
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A 5-week behavioral course for a designated support person (family, friend, other) to the person with GD.
The course focuses on teachings on living with minority stress, maladaptive and adaptive emotion regulation, emotional awareness, validation, interpersonal skills and values.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of participants recruited to I-ER GD.
Time Frame: At pretreatment.
|
Measures will include recruitment rate during study inclusion period (0-30 participants).
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At pretreatment.
|
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Client Satisfaction Questionnaire (CSQ-8; Attkisson & Zwick, 1982) in I-ER GD
Time Frame: At post-treatment (week 12).
|
Measures treatment satisfaction after treatment.
Range 8-32, higher values equals higher satisfaction with treatment.
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At post-treatment (week 12).
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The Credibility and Expectancy Questionnaire (Devilly & Borkovec, 2000) in I-ER GD.
Time Frame: At treatment week 2.
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Measures treatment credibility and expectancy for positive change.
Range 0-5, higher values equals higher treatment credibility and expectancy.
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At treatment week 2.
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The Negative effects Questionnaire (NEQ; Rozental et al. 2016) in I-ER GD.
Time Frame: At post-treatment (week 12).
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Measures negative effects of psychological treatment after an intervention.
Range 0-20, higher values equals worse outcomes, and more negative effects of treatment.
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At post-treatment (week 12).
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The internet intervention Patient Adherence Scale (iiPAS; Lenhard et al. 2019) in I-ER GD
Time Frame: At mid-treatment (week 5).
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Measures adherence to treatment at two timepoints of the treatment.
Range 0-20.
Higher scores indicate better adherence.
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At mid-treatment (week 5).
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The internet intervention Patient Adherence Scale (iiPAS; Lenhard et al. 2019) in I-ER GD
Time Frame: At post-treatment (week 12).
|
Measures adherence to treatment at two timepoints of the treatment.
Range 0-20.
Higher scores indicate better adherence.
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At post-treatment (week 12).
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Number of participants recruited to I-ER SUPPORT.
Time Frame: At pretreatment.
|
Measures will include recruitment rate during study inclusion period (0-15 participants).
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At pretreatment.
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The Client Satisfaction Questionnaire (CSQ-8; Attkisson & Zwick, 1982) in I-ER SUPPORT
Time Frame: At post-treatment (week 10).
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Measures treatment satisfaction.
Range 8-32, higher values equals higher satisfaction with treatment.
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At post-treatment (week 10).
|
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The Credibility and Expectancy Questionnaire (Devilly & Borkovec, 2000) in I-ER SUPPORT
Time Frame: At treatment week 2.
|
Measures treatment credibility and expectancy for positive change.
Range 0-5, higher values equals higher treatment credibility and expectancy.
|
At treatment week 2.
|
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The Negative effects Questionnaire (NEQ; Rozental et al. 2016) in I-ER SUPPORT.
Time Frame: At post-treatment (week 10).
|
Measures negative effects of psychological treatment.
Range 0-20, higher values equals worse outcomes, and more negative effects of treatment.
|
At post-treatment (week 10).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in Gender minority stress and resilience (GMSR, Testa et al 2014) for I-ER GD.
Time Frame: At pre-treatment and at post treatment (week 12)
|
Changes in the Gender minority stress and resilience scale.
Range 0-17 for sub scales Gender related discrimination, rejection, victimization.
Higher values represents higher levels of discrimination, rejection, victimization etc. Range 0-164 for sub scales Non-affirmation of gender identity, Internalized transphobia, Pride, Negative expectations for the future, Nondisclosure and Community connectedness.
Higher values represents higher levels of whatever the sub scale covers (e.g.
pride, internalized transphobia, community connectedness etc).
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At pre-treatment and at post treatment (week 12)
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Changes in The Difficulties in emotion regulation scale, (DERS-16; Gratz & Roemer, 2004) for I-ER GD.
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in the Difficulties in emotion regulation scale, DERS-16.
Range 16-80.
Lower values equals better outcomes.
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At pre-treatment and at post treatment (week 12)
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Changes in The Difficulties in emotion regulation scale, (DERS-16; Gratz & Roemer, 2004) for I-ER GD.
Time Frame: Weekly during the treatment (weeks 1-11)
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Changes in the Difficulties in emotion regulation scale, DERS-16.
Range 16-80.
Lower values equals better outcomes.
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Weekly during the treatment (weeks 1-11)
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Changes in The Emotion Regulation Questionnaire, (ERQ; Gross & John, 2003) for I-ER GD.
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in the Emotion Regulation Questionnaire, ERQ.
Subscales Cognitive reappraisal (Range 6-42).
and Suppression (Range 4-28).
Higher values equals better outcomes in reappraisal, and worse outcomes in Suppression.
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At pre-treatment and at post treatment (week 12)
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Changes inThe Alcohol Use Disorders Identification Test (AUDIT; Berman, Wennberg & Källmén, 2012) for I-ER GD.
Time Frame: At baseline and at post treatment (week 12)
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Changes in alcohol consumption.
Range 0-40 where higher values equal higher substance use, worse outcomes.
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At baseline and at post treatment (week 12)
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Changes inThe Drug Use Disorders Identification Test (DUDIT; Berman, Wennberg & Källmén, 2012) for I-ER GD.
Time Frame: At baseline and at post treatment (week 12)
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Changes in drug consumption.
Range 0-44 where higher values equal higher substance use, worse outcomes.
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At baseline and at post treatment (week 12)
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Changes in Gender Congruence and Life Satisfaction Scale (GCLS; Dhejne et al. 2019) for I-ER GD
Time Frame: At baseline and at post treatment (week 12)
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Change and measure improvements in gender (in)congruence, related mental well-being, and life satisfaction throughout the process of undergoing gender affirming medical interventions.
Range: 38-190 where higher values indicate greater gender congruence, greater gender-related well-being, and greater life satisfaction.
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At baseline and at post treatment (week 12)
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Changes in Work and social adjustment scale (WSAS; Marks 1986) for I-ER GD
Time Frame: At baseline and at post treatment (week 12)
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Changes in functioning.
Ranges from 0-40 where higher scores indicate a more impaired functioning.
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At baseline and at post treatment (week 12)
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Changes in Social Interaction Anxiety Scale (SIAS; Mattick & Clarke 1998) for I-ER GD
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in anxiety over 20 different situations.
Ranges from 0-80 where higher scores indicate a higher social anxiety.
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At pre-treatment and at post treatment (week 12)
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Changes in Social Interaction Anxiety Scale (SIAS; Mattick & Clarke 1998) for I-ER GD
Time Frame: Weekly during the treatment (weeks 1-11)
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Changes in anxiety over 20 different situations.
Ranges from 0-80 where higher scores indicate a higher social anxiety.
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Weekly during the treatment (weeks 1-11)
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Changes in Montgomery Åsberg Depression Rating Scale (MADRS-S; Montgomery & Åsberg 1979) for I-ER GD
Time Frame: At pre-treatment and post treatment (week 12)
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Changes in depressive symptoms.
Ranges from 0-54 where higher scores indicate higher depressive severity.
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At pre-treatment and post treatment (week 12)
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Changes in Deliberate Self-Harm Inventory (DSHI-9; Lundh, Karim & Quillisch 2007) for I-ER GD
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in instances and forms of self-harming behavior.
Higher number of instances indicates worse outcomes.
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At pre-treatment and at post treatment (week 12)
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Changes in Deliberate Self-Harm Inventory (DSHI-9; Lundh, Karim & Quillisch 2007) for I-ER GD
Time Frame: Weekly during the treatment (weeks 1-11)
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Changes in instances and forms of self-harming behavior.
Higher number of instances indicates worse outcomes.
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Weekly during the treatment (weeks 1-11)
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Changes in Brunnsviken Brief Quality of Life Inventory (BBQ; Lindner et al, 2016) for I-ER GD
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in perceived quality of life.
Range: 0-96.
Higher scores indicate a higher perceived quality of life.
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At pre-treatment and at post treatment (week 12)
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Changes in Satisfaction With Life, Swedish (SWLS; Diener 1985) for I-ER GD
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in global cognitive judgements of one's life.
Range: 0-35.
Higher score indicates higher satisfaction with one's life.
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At pre-treatment and at post treatment (week 12)
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Changes in Perceived Stress Scale (PSS-14; Cohen, Kamarck & Mermelstein 1983) for I-ER GD
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in perceived stress.
Range: 0-56.
Higher scores indicate greater perceived stress.
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At pre-treatment and at post treatment (week 12)
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Changes in Multidimensional Scale of Perceived Social Support (MSPSS; Zimet et al, 1988) for I-ER GD
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in perceived support from family, friends and significant other(s).
Range: 12-84.
Higher scores indicate greater perceived stress.
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At pre-treatment and at post treatment (week 12)
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Changes in Rosenberg's scale of self-esteem (Rosenberg; Schmitt & Allik 2005) for I-ER GD
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in self-esteem.
Range: 0-40.
Higher scores indicate higher self-esteem.
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At pre-treatment and at post treatment (week 12)
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Changes in Rumination Response Scale (RRS-10; Nolen-Hoeksema, Morrow 1991) for I-ER GD
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in ruminative tendencies.
Range: 10-40.
Higher scores indicate higher levels of ruminative response styles.
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At pre-treatment and at post treatment (week 12)
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Changes in Affect Labeling Questionnaire (ALQ; Sahi et al, in prep.) for I-ER GD
Time Frame: At pre-treatment and at post treatment (week 12)
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Changes in one's ability to recognize emotions.
Range 12-60.
Higher scores indicates higher ability to recognize and label emotions.
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At pre-treatment and at post treatment (week 12)
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Changes in The Gender/Sex diversity belief scale (GSDB; Schudson & van Anders, 2022) for I-ER SUPPORT
Time Frame: At pre-treatment and at post treatment (week 10)
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Changes in the Gender/Sex diversity belief scale.
Range 23-161.
Higher values equals more positive attitudes toward transgender individuals.
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At pre-treatment and at post treatment (week 10)
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Changes in Affect Labeling Questionnaire (ALQ; Sahi et al, in prep.) for I-ER SUPPORT
Time Frame: At pre-treatment and at post treatment (week 10)
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Changes in one's ability to recognize emotions.
Range 12-60.
Higher scores indicates higher ability to recognize and label emotions.
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At pre-treatment and at post treatment (week 10)
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Changes in The Emotion Regulation Questionnaire, (ERQ; Gross & John, 2003) for I-ER SUPPORT.
Time Frame: At pre-treatment and at post treatment (week 10)
|
Changes in the Emotion Regulation Questionnaire, ERQ.
Subscales Cognitive reappraisal (Range 6-42).
and Suppression (Range 4-28).
Higher values equals better outcomes in reappraisal, and worse outcomes in Suppression.
|
At pre-treatment and at post treatment (week 10)
|
|
Changes in The Difficulties in emotion regulation scale, (DERS-16; Gratz & Roemer, 2004) for I-ER SUPPORT
Time Frame: At pre-treatment and at post treatment (week 10)
|
Changes in the Difficulties in emotion regulation scale, DERS-16.
Range 16-80.
Lower values equals better outcomes.
|
At pre-treatment and at post treatment (week 10)
|
|
Changes in The Difficulties in emotion regulation scale, (DERS-16; Gratz & Roemer, 2004) for I-ER SUPPORT
Time Frame: Weekly during the treatment (weeks 1-10)
|
Changes in the Difficulties in emotion regulation scale, DERS-16.
Range 16-80.
Lower values equals better outcomes.
|
Weekly during the treatment (weeks 1-10)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hanna Sahlin, PhD, Karolinska Institutet
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022-00577-01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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