- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02227160
Group Interventions for Suicidal African Americans
The investigator is conducting a hybrid efficacy-effectiveness randomized controlled trial with low-income African American suicide attempters. Guided by the Theory of Triadic Influence (TTI), this pilot randomized controlled trial aims:
- to determine if psychosocial group intervention (PGI) is more effective than enhanced treatment as usual (ETAU) in reducing suicidal behavior (ideation, attempts; primary outcome) and improving its correlates (depressive symptoms, hopelessness, quality of life) (secondary outcomes) in low-income African Americans with a recent attempt.
- to determine if PGI is more effective than ETAU at bolstering intrapersonal (I), social/situational (SS), and cultural/environmental (CE) risk and protective factors that mediate the condition-suicidal behavior and correlates link and thus serve as mechanisms of change.
- to determine I, SS, and CE variables that moderate the condition-suicidal behavior link and thus serve as predictors of intervention outcome.
Hypothesis for Aim 1: At post-intervention and follow-up, PGI participants will evidence greater improvements in suicidal behavior and its correlates than those in ETAU.
Hypothesis for Aim 2: Changes in these risk and protective factors will account for condition effects on outcomes: (1) psychological distress, aggression, impulsivity, substance abuse, low self-esteem, and suicide acceptability (I-risk); (2) perceived burdensomeness and thwarted belongingness, relationship discord, intimate partner violence perpetration and victimization (SS-risk); (3) access to a weapon and barriers to service utilization (CE-risk); (4) reasons for living, optimism, positive ethnic identity, effective coping, and spiritual well-being (I-protective); (5) overall family health and social support from family and friends (SS-protective); and (6) religious involvement and effectiveness of obtaining resources (CE-protective).
Hypothesis for Aim 3: Individuals (1) having fewer Diagnostic and Statistical Manual of Mental Disorders (DSM) disorders and attachment styles characterized by positivity toward the self and others (I); (2) children and more limited trauma histories (SS); and (3) more daily hassles and less exposure to community disorder (CE) will evidence greater reductions in suicidal behavior and its correlates and greater enhancements in quality of life at post-intervention and follow-up.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Attention will be paid to Theory of Triadic Influence intrapersonal, social/ situational, and cultural/ environmental risk and protective factors that impact outcomes. The central hypothesis is that compared to enhanced treatment as usual, through targeting Theory of Triadic Influence-risk and protective factors the culturally-informed, Theory of Triadic Influence-driven, empowerment based psychosocial group intervention will more positively alter trajectories in suicidal behaviors and its correlates. The rationale is that upon study completion, if data support the psychosocial group intervention value, they will facilitate our long-term goal of disseminating evidence-based culturally-relevant interventions.
In order to test the hypothesis that at post-intervention and 6 and 12-month follow-up, compared to individuals in ETAU, those in the PGI will endorse less I, SS, and CE risk factors, reduced suicidal ideation, depressive symptoms, and hopelessness, and greater levels of I, SS, and CE protective factors as well as increased quality of life, the study procedures will be as follows: Male and female participants between the ages of 18-64 will be recruited in the medical and psychiatric emergency rooms at GHS. Once the individual has been medically cleared and has provided informed consent, he/she will be screened for study appropriateness by trained project team members (10-20 minutes). If he/she meets inclusion criteria, study participation will include a 3-hour interview. All study measures will be read to each participant. Measures will assess background variables, suicidal behavior, depressive symptoms, hopelessness, quality of life, and I, SS, and CE risk and protective factors. All measures are psychometrically sound and appropriate for use with an African American population. Once the interview is over, the participant will be randomly assigned to either the PGI (10 group therapy sessions) or the ETAU condition (participation in a support group focused on suicidal behaviors plus suicidal behavior monitoring and help with accessing resources). The PGI, conducted in accord with the culturally informed, TTI-guided, and empowerment based group protocol, and the support group will be unstructured; both groups will last 120 minutes. Following the completion of the PGI or ETAU condition, the individuals will be assessed at post-intervention (3 hours), and at 6 month and 12 month follow-ups (3 hours each). To increase retention and reduce suicide risk, reminder phone calls will be made and texts sent on Relieflink, a suicide prevention app that received 1st prize in an App Challenge sponsored by Substance Abuse and Mental Health Services Administration.
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Georgia
-
Atlanta, Georgia, United States, 30303
- Grady Memorial Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 18 - 64 yrs old
- patients who seek treatment at Grady Health System (GHS) after a suicide attempt
- African American
- speak English
Exclusion Criteria:
- cognitive impairments
- medical instability
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Psychosocial group intervention
Subjects will seek outpatient counseling, support groups, in addition to 10 weekly group meetings
|
10 weekly group meetings with up to five other men and women at Grady Health System
Usual mental health care
|
|
Active Comparator: Control
Subjects will seek outpatient counseling and support groups only
|
Usual mental health care
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in scores on Beck Scale for Suicidal Ideation
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Beck Scale for Suicidal Ideation is a 21-item instrumentation used to measure the current intensity of patients' specific attitudes, behaviors and plans to commit suicide.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in scores on Beck Depression Inventory - II
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Beck Depression Inventory - II is a 21-item, self-reported questionnaire used to assess characteristics of depression.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Beck Hopelessness Scale
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Beck Hopelessness Scale is a 20-item true-false self-report scale that measures the level of negative expectations about the future held by respondents
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on WHO Quality of Life Brief Instrument
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
The WHOQOL-BREF instrument comprises 26 items, which measure the following broad domains: physical health, psychological health, social relationships, and environment.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Patient Satisfaction
Time Frame: 12 months
|
Intervention Satisfaction Survey (ISS)
|
12 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in the Symptom Checklist 90-Revised (SCL 90-R) scale
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Symptom Checklist 90-Revised (SCL 90-R) questionnaire measures overall levels of psychological and physical functioning.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores for Alcohol Use Disorders Identification Test
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Alcohol Use Disorders Identification Test (AUDIT) is a 10 question test to determine if a person's alcohol consumption may be harmful
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Drug Abuse Screening Test
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Drug Abuse Screening Test (DAST) is a 28-item self-report scale that is used as a screening instrument for the abuse of drugs other than alcohol.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Rosenberg Self-Esteem Scale (RSE)
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
A 10-item scale that measures global self-worth by measuring both positive and negative feelings about the self.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Changes in scores on Short Form Buss-Perry Aggression Questionnaire
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Short Form Buss-Perry Aggression Questionnaire is a 12-item short form that assesses four aspects of aggressive behavior: physical aggression, verbal aggression, anger and hostility.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Changes in scores on Barratt Impulsiveness Scale
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Barratt Impulsiveness Scale is a 30-item self-report questionnaire designed to assess general impulsiveness taking into account the multifactorial nature of the construct.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Suicide Acceptability Scale
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Suicide Acceptability Scale is an 8-item measure of suicide acceptability
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Changes in scores on Interpersonal Needs Questionnaire (INQ)
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Interpersonal Needs Questionnaire (INQ) is a 15-item self-report measure of the constructs of thwarted belongingness and perceived burdensomeness as defined by the Interpersonal Theory of Suicide.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Dyadic Adjustment Scale
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Dyadic Adjustment Scale is a 32-item self-report tool used to assess couple satisfaction and to evaluate how each partner within the couple perceives his or her relationship
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Conflict Tactics Scale-Revised
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Conflict Tactics Scale-Revised (CTS-2) is 78-item, self-administered questionnaire that assesses both positive and negative behaviors used in response to conflict between romantic partners in the past year
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Clinical Demographic Questionnaire
Time Frame: Baseline
|
Demographic questionnaire assesses demographic information as well as information regarding to access to weapons
|
Baseline
|
|
Change in scores on Reasons for Living Inventory
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Reasons for Living Inventory contains 12 possible reasons for living, which respondents rate regarding the importance each item would be for living if suicide were contemplated.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Life Orientation Test - Revised
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Life Orientation Test - Revised is a 10-item test assessing generalized positive outcome expectancies
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Multi-dimensional Inventory of Black Identity
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
The Multi-dimensional Inventory of Black Identity is designed to assess the three cross-situationally stable dimensions (Centrality, Regard, and Ideology)
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Ways of Coping (Revised) Questionnaire
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Ways of Coping (Revised) is self-reported questionnaire used to assess adaptive and maladaptive ways to cope with negative emotions or problematic situations
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Africultural Coping Systems Inventory
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Africultural Coping Systems Inventory is a 30-item measure of the culture-specific coping strategies used by African Americans in stressful situations and is grounded in an African-centered conceptual framework
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Barriers to Accessing Services Scale
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
|
Change in scores on Spiritual Well-Being Scale
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Spiritual Well-Being Scale is a 20-item scale used for the assessment of both individual and congregational spiritual well-being
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Family Assessment Device
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Family Assessment Device is a 53 item questionnaire designed to evaluate families.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Social Support Behaviors Scale
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Social Support Behaviors Scale is designed to assess supportive behavior available from family and from friends.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Changes in scores on Multidimensional Measure of Religious Involvement for African Americans
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Multidimensional Measure of Religious Involvement for African Americans is a 12-item scale measuring religious indicators.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in score on Effectiveness of Obtaining Resources questionnaire
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
|
Change in evaluation on Structured Clinical Interview for DSM-5-Research Version
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Structured Clinical Interview for DSM-5-Research Version is semi-structured interview that allows researchers to make clinical diagnoses according to DSM criteria
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in evaluation on Structured Clinical Interview for DSM-PD
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
The Structured Clinical Interview for DSM-PD is a semi-structured interview for making DSM-IV Axis II: Personality Disorder diagnoses
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Relationship Scales Questionnaire
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Relationship Scales Questionnaire is a scale that consists of 17 items to assess attachment patterns.
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Childhood Trauma Questionnaire - Short Form (CTQ-SF)
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
The CTQ-SF is a 28-item self-report instrument for adults and adolescents that assesses retrospective child abuse and neglect
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Survey of Recent Life Experiences scale
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Survey of Recent Life Experiences is a 51-item self-report instrument that measures hassles for adults
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
|
Change in scores on Community Disorder Scale
Time Frame: Baseline, post-therapy, 6 months and 12 months after therapy
|
Baseline, post-therapy, 6 months and 12 months after therapy
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Nadine Kaslow, PhD, Emory University
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
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
- IRB00073021
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 Depression
-
Massachusetts General HospitalRecruitingDepression | Depression - Major Depressive Disorder | Depression Chronic | Depression in Adults | Depression Disorders | Depression DisorderUnited States
-
University of California, San FranciscoNational Center for Complementary and Integrative Health (NCCIH)Active, not recruitingDepression Moderate | Depression Mild | Depression, TeenUnited States
-
ProgenaBiomeWithdrawnDepression | Depression, Postpartum | Depression, Anxiety | Depression Moderate | Depression Severe | Clinical Depression | Depression in Remission | Depression, Endogenous | Depression ChronicUnited States
-
Sorlandet Hospital HFUniversity of Oslo; Karolinska Institutet; Australian Catholic University; Helse...RecruitingAnxiety | Anxiety Depression | Depression Anxiety Disorder | Depression - Major Depressive DisorderNorway
-
Lipocine Inc.CompletedDepression, Postpartum | Postnatal Depression | Peripartum Depression | Depression, Post-Partum | Postpartum Depression (PPD) | Post-Natal DepressionUnited States
-
Washington University School of MedicineCompletedTreatment Resistant Depression | Late Life Depression | Geriatric Depression | Refractory Depression | Therapy-Resistant DepressionUnited States, Canada
-
Kintsugi Mindful Wellness, Inc.Sonar Strategies; Kolby Walker, DO; Brittany KimbleRecruitingDepression | Depression Moderate | Depression Severe | Depression MildUnited States
-
Kintsugi Mindful Wellness, Inc.Sonar Strategies; Vituity PsychiatryActive, not recruitingDepression | Depression Moderate | Depression Severe | Depression MildUnited States
-
University of MinnesotaCompletedDepression SymptomsUnited States
-
Bekelu Teka WorkuJimma UniversityNot yet recruitingPrenatal Depression | Mental Health Related Quality of Life | Maternal Postpartum Depression | Paternal Postpartum DepressionEthiopia
Clinical Trials on 10 weekly group meetings
-
Helsinki University Central HospitalUniversity of Helsinki; Occupational Health HelsinkiActive, not recruiting
-
M.D. Anderson Cancer CenterNational Cancer Institute (NCI)TerminatedProstate CancerUnited States
-
Université Catholique de LouvainRecruitingMultiple Chronic ConditionsBelgium
-
Meir Medical CenterCompletedOsteoarthritis | Low Back PainIsrael
-
University of MinnesotaCompletedOverweight | ObeseUnited States
-
Duke UniversityCompletedPreterm BirthUnited States
-
Sophiahemmet UniversityKarolinska Institutet; Uppsala University; Arizona State UniversityCompletedType 2 Diabetes | PrediabetesSweden
-
University of Colorado, DenverCompletedOsteoarthritisUnited States
-
Medical University InnsbruckRecruitingMigraine | Headache Disorders | Pediatric MigraineAustria
-
University of Massachusetts, WorcesterBinghamton University; National Institute on Disability, Independent Living... and other collaboratorsCompletedEducational Problems | Mental ImpairmentUnited States