Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05509166

Affirmative Psychotherapy for Sexual Minority Women's Mental and Behavioral Health

The purpose of this 2-arm randomized controlled trial is to assess the efficacy of a 10-session lesbian, gay, bisexual, transgender, and queer (LGBTQ)-affirmative cognitive-behavioral psychotherapy (CBT) delivered via telehealth in a large sample of sexual minority women (SMW) in New York, New Jersey and Pennsylvania. The investigators will assess whether the EQuIP (Empowering Queer Identities in Psychotherapy) treatment demonstrates significant reductions in heavy drinking (HD) and mental health symptoms (e.g., depression) compared to LGBTQ-affirmative treatment-as-usual.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Yale LGBTQ Mental Health Initiative with the Yale School of Public Office

New York, 10001, United States

Location status: Recruiting

Location contact

Ben E Eisenstadt, BA

CONTACT

[email protected]

347-633-0610

Danielle M Chiaramonte, PhD

CONTACT

[email protected]

708-334-8331

John E Pachankis, PhD

PRINCIPAL_INVESTIGATOR

About this study

The purpose of this study is to assess the efficacy of a 10-session LGBTQ-affirmative cognitive behavioral psychotherapy (CBT) delivered via telehealth in a large sample of sexual minority women (SMW) in New York, New Jersey and Pennsylvania. The treatment, EQuIP (Empowering Queer Identities in Psychotherapy), uses a CBT-based transdiagnostic approach to target the common cognitive, affective, and behavioral responses to minority stress that lead to mental and behavioral health disparities for sexual minority women. We will assess in a 2-arm randomized controlled trial (RCT) whether the EQuIP treatment demonstrates significant reductions in heavy drinking (HD) and mental health symptoms (e.g., depression) compared to LGBTQ-affirmative Treatment-As-Usual. The investigators will assess whether psychosocial mechanisms (e.g., emotion dysregulation) mediate reductions in heavy drinking and separately and identify whether EQuIP is differentially efficacious across key demographic factors.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • be 18 years of age or older
  • be fluent in English
  • self-identify as lesbian, bisexual, queer, pansexual, or other non-heterosexual identity
  • report at ≥ 8 standard drinks/week, on average, in the past 30 days, OR report at least 2 heavy drinking days ( ≥ 4 drinks in one day) in the past 30 days 4) currently experience a Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 depression or anxiety disorder (screened initially using a cutoff of ≥ 2 on the Brief Symptom Inventory-4 and further confirmed by diagnostic interview via the DIAMOND) 5) report at least minimum motivation to reduce drinking (measured by the Readiness Ruler) 6) live in New York, New Jersey, and Pennsylvania and planning to stay for at least the next 4 months

Exclusion criteria

  • report current mental health treatment ≥1 day/mo
  • report having received any CBT in the past 3 months
  • report current alcohol or drug abuse treatment, except mutual self-help (e.g., Alcoholics Anonymous)
  • need alcohol detoxification indicated by ≥9 on Clinical Institute Withdrawal Assessment for Alcohol-Revised (CIWA-Ar)
  • exhibit active psychosis or active mania, as assessed by the Structured Clinical Interviews for DSM-5 Disorders (SCID) Psych Screen
  • exhibit active suicidality or active homicidality, as assessed by the SCID-Psych Screen
  • be currently legally mandated to attend treatment
  • demonstrate gross cognitive impairment, as assessed with the Telephone Interview for Cognitive Status

Treatment and study plan

LGBTQ-affirmative Cognitive Behavioral Therapy

Behavioral

10-session LGBTQ-affirmative psychotherapy using CBT techniques

LGBTQ-affirmative Treatment-As-Usual

Behavioral

10-session LGBTQ-affirmative psychotherapy

Primary outcomes

  1. Change in heavy drinking

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The proportion of heavy drinking days will be assessed using a 30-day Timeline Followback. The Timeline Followback is a structured interview that will assess alcohol use over the past 30 days. Heavy drinking days are defined as those in which more than four drinks were consumed within a two-hour period.

Secondary outcomes

  1. Diagnostic Interview for Anxiety, Mood, and OCD and Related Neuropsychiatric Disorders (DIAMOND)

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The (DIAMOND) is a semi-structured diagnostic interview based on the DSM-5 that enables non-clinicians to determine the presence and severity of mood, anxiety, and stress-/trauma-related disorders.

  2. Depression Symptom Severity

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Center for Epidemiological Studies - Depression Scale (CES-D) will be used to compute an overall depression score (sum of the 20 items, with Items 3, 11, 14, and 16 reverse-scored). A higher score will indicate more depressive symptomatology during the past week. The range of scores for this outcome is 0-60.

  3. Anxiety Symptom Severity

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Beck Anxiety Inventory (BAI) will be used to compute an overall anxiety score. Total score is calculated by finding the sum of the 21 items. Score of 0-21 = low anxiety; score of 22-36 = moderate anxiety; score of 36 and above = high anxiety. A higher score will indicate more depressive symptomatology during the past week. The range of scores for this outcome is 0-63.

  4. Overall Depression Severity and Impairment Scale (ODSIS)

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Overall Depression Severity and Impairment Scale (ODSIS) will be used to compute an overall depression severity and impairment score. Total score is calculated using the sum of the 5 items. The range of scores for this outcome is 0-20.

  5. Overall Anxiety Severity and Impairment Scale (OASIS)

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Overall Anxiety Severity and Impairment Scale (OASIS) will be used to compute an overall anxiety severity and impairment score. Total score is calculated using the sum of the 5 items. The range of scores for this outcome is 0-20.

  6. PTSD symptoms

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The PTSD Checklist for DSM-5 (PCL-5) is a 20-item self-report measure that assesses the 20 DSM-5 symptoms of PTSD to monitor symptom change during and after treatment

  7. Suicidal Ideation

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Suicidal Ideation Attributes Scale (SIDAS) is a 5-item self-report measure that assesses suicidal ideation with response options from 0 to 10. Total SIDAS scores are calculated as the sum of the five items, with controllability reverse scored. Total scores range from 0 to 50.

  8. Mental Health Symptom Presence and Severity

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Brief Symptom Inventory (BSI) measures current or past presence and severity of mental health symptoms. The self-report measure is rated on a scale of 0 (not at all) to 4 (extremely), with higher scores indicating more severe symptomatology.

  9. Alcohol Use

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Patient Reported Outcomes Measurement Information System (PROMIS) Alcohol Use Short Form is a self-report questionnaire designed to measure alcohol use in the past 30 days. Participants respond to 7 questions on a scale of 1 (Never) to 5 (Almost Always), and the sum of the responses are converted to a t-score, with a higher score representing higher alcohol use

  10. Effects of Alcohol Use

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Brief Comprehensive Effects of Alcohol Scale evaluates participants' outcome expectancy when drinking. The measure contains 38 items that are rated on a scale of 1 (Disagree) to 4 (Agree), with a higher sum indicating a higher level of effect in certain alcohol use domains.

  11. Frequency of Alcohol Use

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Daily Drinking Questionnaire assesses the amount of drinks a participant consumes on a daily basis throughout the course of a week.

  12. Alcohol Self-Efficacy

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Alcohol Abstinence Self-Efficacy Scale measures a participant's confidence in being able to avoid or abstain from alcohol. Participants rate 20 items on a scale of 1 (Not at all confident) to 5 (Extremely confident), with a higher score indicating higher confidence in being able to abstain from alcohol.

  13. Drug Use and Drug-Related Problems

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Drug Use Disorders Identification Test (DUDIT) is a self-report measure designed to assess drug-related problems and drug use. Participants rate 11 items that can be scored on a scale of 0 to 4, with a higher sum representing more drug-related problems and dependency.

  14. Cannabis Use and Cannabis-Related Problems

    Time frame: Baseline, 4-month follow-up, 8-month follow-up, and 12-month follow-up

    The Cannabis Use Disorder Identification Test (CUDIT) assesses self-reported cannabis use and problems related to cannabis use. Participants rate 10 items on varying scales, with a higher sum indicating higher cannabis use and related problems.

Study contacts

Contact information is provided by the study sponsor or research team.

Danielle M Chiaramonte, PhD

CONTACT

[email protected]

708-334-8331

John E Pachankis, PhD

CONTACT

[email protected]

646-429-9407

Sponsors and collaborators

Lead sponsor

Yale University

Other

Collaborators

  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Registry information

Official study title

A Unified Protocol to Address Sexual Minority Women's Minority Stress, Mental Health and Hazardous Drinking

Acronym: EQuIP

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Aug 22, 2022
Registry last updated
Jul 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.