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Clinical Trials/NCT05534763
NCT05534763
Completed
N/A

Internet-delivered Emotion Regulation Treatment (I-ER GD) for Transgender Adults and Co-occurring Mental Health Problems

Karolinska Institutet1 site in 1 country24 target enrollmentAugust 24, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Gender Dysphoria
Sponsor
Karolinska Institutet
Enrollment
24
Locations
1
Primary Endpoint
The Negative effects Questionnaire (NEQ; Rozental et al. 2016) in I-ER GD.
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

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

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.

Registry
clinicaltrials.gov
Start Date
August 24, 2022
End Date
June 30, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hanna Sahlin

Principal investigator

Karolinska Institutet

Eligibility Criteria

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.

Outcomes

Primary Outcomes

The Negative effects Questionnaire (NEQ; Rozental et al. 2016) in I-ER GD.

Time Frame: At post-treatment (week 12).

Measures negative effects of psychological treatment after an intervention. Range 0-20, higher values equals worse outcomes, and more negative effects of treatment.

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.

Number of participants recruited to I-ER GD.

Time Frame: At pretreatment.

Measures will include recruitment rate during study inclusion period (0-30 participants).

Number of participants recruited to I-ER SUPPORT.

Time Frame: At pretreatment.

Measures will include recruitment rate during study inclusion period (0-15 participants).

The Client Satisfaction Questionnaire (CSQ-8; Attkisson & Zwick, 1982) in I-ER SUPPORT

Time Frame: At post-treatment (week 10).

Measures treatment satisfaction. Range 8-32, higher values equals higher satisfaction with treatment.

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.

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.

The Credibility and Expectancy Questionnaire (Devilly & Borkovec, 2000) in I-ER GD.

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.

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.

Secondary Outcomes

  • Changes in Deliberate Self-Harm Inventory (DSHI-9; Lundh, Karim & Quillisch 2007) for I-ER GD(Weekly during the treatment (weeks 1-11))
  • Changes in The Difficulties in emotion regulation scale, (DERS-16; Gratz & Roemer, 2004) for I-ER GD.(Weekly during the treatment (weeks 1-11))
  • Changes inThe Drug Use Disorders Identification Test (DUDIT; Berman, Wennberg & Källmén, 2012) for I-ER GD.(At baseline and at post treatment (week 12))
  • Changes in Social Interaction Anxiety Scale (SIAS; Mattick & Clarke 1998) for I-ER GD(Weekly during the treatment (weeks 1-11))
  • Changes in Perceived Stress Scale (PSS-14; Cohen, Kamarck & Mermelstein 1983) for I-ER GD(At pre-treatment and at post treatment (week 12))
  • Changes in Montgomery Åsberg Depression Rating Scale (MADRS-S; Montgomery & Åsberg 1979) for I-ER GD(At pre-treatment and post treatment (week 12))
  • Changes inThe Alcohol Use Disorders Identification Test (AUDIT; Berman, Wennberg & Källmén, 2012) for I-ER GD.(At baseline and at post treatment (week 12))
  • Changes in Brunnsviken Brief Quality of Life Inventory (BBQ; Lindner et al, 2016) for I-ER GD(At pre-treatment and at post treatment (week 12))
  • Changes in Rumination Response Scale (RRS-10; Nolen-Hoeksema, Morrow 1991) for I-ER GD(At pre-treatment and at post treatment (week 12))
  • Changes in Affect Labeling Questionnaire (ALQ; Sahi et al, in prep.) for I-ER GD(At pre-treatment and at post treatment (week 12))
  • Changes in Gender minority stress and resilience (GMSR, Testa et al 2014) for I-ER GD.(At pre-treatment and at post treatment (week 12))
  • Changes in The Emotion Regulation Questionnaire, (ERQ; Gross & John, 2003) for I-ER GD.(At pre-treatment and at post treatment (week 12))
  • Changes in Gender Congruence and Life Satisfaction Scale (GCLS; Dhejne et al. 2019) for I-ER GD(At baseline and at post treatment (week 12))
  • Changes in Work and social adjustment scale (WSAS; Marks 1986) for I-ER GD(At baseline and at post treatment (week 12))
  • Changes in The Difficulties in emotion regulation scale, (DERS-16; Gratz & Roemer, 2004) for I-ER SUPPORT(Weekly during the treatment (weeks 1-10))
  • Changes in Satisfaction With Life, Swedish (SWLS; Diener 1985) for I-ER GD(At pre-treatment and at post treatment (week 12))
  • Changes in Multidimensional Scale of Perceived Social Support (MSPSS; Zimet et al, 1988) for I-ER GD(At pre-treatment and at post treatment (week 12))
  • Changes in Rosenberg's scale of self-esteem (Rosenberg; Schmitt & Allik 2005) for I-ER GD(At pre-treatment and at post treatment (week 12))
  • Changes in The Gender/Sex diversity belief scale (GSDB; Schudson & van Anders, 2022) for I-ER SUPPORT(At pre-treatment and at post treatment (week 10))
  • Changes in Affect Labeling Questionnaire (ALQ; Sahi et al, in prep.) for I-ER SUPPORT(At pre-treatment and at post treatment (week 10))
  • Changes in The Emotion Regulation Questionnaire, (ERQ; Gross & John, 2003) for I-ER SUPPORT.(At pre-treatment and at post treatment (week 10))

Study Sites (1)

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