search
Back to results

Digital Mental Health Intervention for Nonsuicidal Self-Injury in Young Adults

Primary Purpose

Nonsuicidal Self Injury, Suicidal Ideation, Depression

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Self-guided digital intervention for NSSI
Digital intervention for NSSI with coaching
Active control
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nonsuicidal Self Injury focused on measuring Digital Mental Health, Nonsuicidal Self Injury, mHealth, Mobile phone, Smartphone, Coach, Conversational Agent

Eligibility Criteria

18 Years - 24 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Ages 18-24 *The age to provide consent in Nebraska is 19. Individuals recruited from the state of Nebraska must be 19 or older.
  • Current NSSI, defined as self-injury on 2 or more days in the past month
  • Has a smartphone
  • English language skills sufficient to engage in the consent and intervention procedures

Exclusion Criteria:

  • Serious mental illness for which intervention would be contraindicated (e.g., psychotic disorder, manic episode, etc.)
  • Severe suicidality (i.e., experiencing suicidal ideation with a plan and intent to act)
  • Current engagement in psychotherapy

Sites / Locations

  • Northwestern University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Self-guided digital intervention for NSSI

Digital intervention for NSSI with coaching

Active control

Arm Description

The self-guided digital intervention for NSSI will consist of 8 weekly modules containing psychoeducation and skill-based practice, and daily ecological momentary assessments. All content is delivered by a highly interactive conversational agent that guides users through the app content via a text-like interface.

The self-guided digital intervention for NSSI will consist of 8 weekly modules containing psychoeducation and skill-based practice, and daily ecological momentary assessments. All content is delivered by a highly interactive conversational agent that guides users through the app content via a text-like interface. This arm will additionally receive lightweight coaching which consists of a one 20-30 minute engagement call at the beginning of treatment. Thereafter, coaches will check in with participants via medium of participants choice twice per week and respond to patient texts, calls, or emails.

The active control arm will receive 8 weekly modules with psychoeducational components only, without the interaction features or EMA for personalization.

Outcomes

Primary Outcome Measures

Alexian Brothers Assessment of Self-Injury - Methods checklist
16-item checklist that assesses the frequency (days/times) of common NSSI methods within the past month.
Alexian Brothers Urges to Self-Injure Scale
5-item self-report measure assessing the intensity and frequency of NSSI urges. Higher scores mean more intense urges to self-injure. Minimum score: 0; maximum score: 30.

Secondary Outcome Measures

Patient Health Questionnaire-9
10-item self-report measure assessing depression symptom severity. Higher scores mean greater symptom severity. Minimum score: 0; maximum score: 27.
Generalized Anxiety Disorder-7
8-item self-report measure assessing generalized anxiety disorder symptom severity. Higher scores mean greater symptom severity. Minimum score: 0; maximum score: 21.
Borderline Evaluation of Severity Over Time
15-item self-report measure assessing borderline symptom severity. Higher scores mean greater symptom severity. Three domains: Thoughts and Feelings, Behaviors-Negative, Behaviors-Positive. Minimum score: 12; maximum score: 72.
Depression Symptom Inventory - Suicidality Subscale
4-item self-report questionnaire assessing the frequency and intensity of suicidal thoughts over previous two weeks. Higher scores signal greater frequency and severity of suicidal thoughts. Minimum score: 0; maximum score: 12.

Full Information

First Posted
April 4, 2022
Last Updated
January 9, 2023
Sponsor
Northwestern University
search

1. Study Identification

Unique Protocol Identification Number
NCT05325944
Brief Title
Digital Mental Health Intervention for Nonsuicidal Self-Injury in Young Adults
Official Title
Digital Mental Health Intervention for Nonsuicidal Self-Injury in Young Adults
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 1, 2024 (Anticipated)
Primary Completion Date
December 1, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a feasibility trial of a digital mental health intervention aimed at young adults (ages 18-25) with nonsuicidal self-injury and who are not currently engaged in mental health treatment. We will pilot three arms: a self-guided DMHI, the DMHI with low-intensity coaching, or an active control which will involve the delivery of non-interactive psychoeducational content via the same app interface. The primary goals of this project are to evaluate the feasibility of the intervention and trial procedures in preparation for a fully-powered randomized-controlled trial.
Detailed Description
The primary purpose of this trial is to test the feasibility of conducting a randomized controlled trial (RCT) of an 8-week digital mental health intervention (DMHI) for non-treatment engaged young adults with repeated nonsuicidal self-injury. The DMHI will be a highly interactive conversational agent that conveys psychoeducational content and guides participants through skill-based activities. We will conduct a 3-arm feasibility trial, randomizing participants to receive the self-guided DMHI, the DMHI with low-intensity coaching, or an active control which will involve the delivery of non-interactive psychoeducational content via the same app interface. Initial randomization will be generated in permuted blocks of 6 using a computer program, with participants assigned on a 1:1:1 ratio. To prevent allocation bias, randomization will be conducted by the biostatistician, who will not inform the study team of the treatment arms until the baseline assessment has been completed and the patient has been enrolled. The control group will serve as the reference group to verify the effectiveness of the DMHI while the comparison of self-guided to coached deployments will evaluate the added benefit of coaching. The primary clinical outcome measures will be frequency of NSSI behavior (ABASI) and frequency of NSSI urges (ABUSI). Secondary outcomes will include suicidal ideation (DSI-SS), depressive symptom severity (PHQ-9), and anxiety symptom severity (GAD-7). This study will enroll individuals who have meet the following eligibility criteria: 1) current NSSI, defined as 2+ self-injury episodes (e.g., cutting, burning) in the past month; 2) Age 18 to 24; 3) English language skills sufficient to engage in the consent and intervention procedures. Participants will be excluded if they 1) Have a severe mental illness diagnosis (e.g., psychotic disorder); 2) Are imminently suicidal, with a plan and intent; or 3) Are currently receiving psychotherapy. Coaching will consist of providing users with support and accountability via positive reinforcement, goal and expectation setting, and monitoring. Coaching outreach will focus on adherence to the treatment but will not provide treatment advice. Coaches will provide a brief (20-30 minute phone call or equivalent depending on the medium) engagement phone call. Thereafter, coaches will check in with participants via messaging, phone call, or email, twice per week and respond to patient messages.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nonsuicidal Self Injury, Suicidal Ideation, Depression, Anxiety
Keywords
Digital Mental Health, Nonsuicidal Self Injury, mHealth, Mobile phone, Smartphone, Coach, Conversational Agent

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Self-guided digital intervention for NSSI
Arm Type
Experimental
Arm Description
The self-guided digital intervention for NSSI will consist of 8 weekly modules containing psychoeducation and skill-based practice, and daily ecological momentary assessments. All content is delivered by a highly interactive conversational agent that guides users through the app content via a text-like interface.
Arm Title
Digital intervention for NSSI with coaching
Arm Type
Experimental
Arm Description
The self-guided digital intervention for NSSI will consist of 8 weekly modules containing psychoeducation and skill-based practice, and daily ecological momentary assessments. All content is delivered by a highly interactive conversational agent that guides users through the app content via a text-like interface. This arm will additionally receive lightweight coaching which consists of a one 20-30 minute engagement call at the beginning of treatment. Thereafter, coaches will check in with participants via medium of participants choice twice per week and respond to patient texts, calls, or emails.
Arm Title
Active control
Arm Type
Active Comparator
Arm Description
The active control arm will receive 8 weekly modules with psychoeducational components only, without the interaction features or EMA for personalization.
Intervention Type
Behavioral
Intervention Name(s)
Self-guided digital intervention for NSSI
Intervention Description
Psychoeducational content, skill-based practice, and daily ecological momentary assessments will be delivered over an 8-week period. Psychological strategies center on cognitive behavioral principles and acceptance-based emotional regulation strategies. Daily EMAs assess NSSI and use of cognitive, behavioral, and emotion regulatory strategies.
Intervention Type
Behavioral
Intervention Name(s)
Digital intervention for NSSI with coaching
Intervention Description
Psychoeducational content and psychological strategies center on cognitive behavioral principles and acceptance-based emotional regulation strategies. Daily EMAs assess NSSI and use of cognitive, behavioral, and emotion regulatory strategies. Human coaching will be used to support intervention use and engagement twice per week via text, call or email.
Intervention Type
Behavioral
Intervention Name(s)
Active control
Intervention Description
Psychoeducational content and psychological strategies center on cognitive behavioral principles and acceptance-based emotional regulation strategies.
Primary Outcome Measure Information:
Title
Alexian Brothers Assessment of Self-Injury - Methods checklist
Description
16-item checklist that assesses the frequency (days/times) of common NSSI methods within the past month.
Time Frame
16 weeks
Title
Alexian Brothers Urges to Self-Injure Scale
Description
5-item self-report measure assessing the intensity and frequency of NSSI urges. Higher scores mean more intense urges to self-injure. Minimum score: 0; maximum score: 30.
Time Frame
16 weeks
Secondary Outcome Measure Information:
Title
Patient Health Questionnaire-9
Description
10-item self-report measure assessing depression symptom severity. Higher scores mean greater symptom severity. Minimum score: 0; maximum score: 27.
Time Frame
16 weeks
Title
Generalized Anxiety Disorder-7
Description
8-item self-report measure assessing generalized anxiety disorder symptom severity. Higher scores mean greater symptom severity. Minimum score: 0; maximum score: 21.
Time Frame
16 weeks
Title
Borderline Evaluation of Severity Over Time
Description
15-item self-report measure assessing borderline symptom severity. Higher scores mean greater symptom severity. Three domains: Thoughts and Feelings, Behaviors-Negative, Behaviors-Positive. Minimum score: 12; maximum score: 72.
Time Frame
16 weeks
Title
Depression Symptom Inventory - Suicidality Subscale
Description
4-item self-report questionnaire assessing the frequency and intensity of suicidal thoughts over previous two weeks. Higher scores signal greater frequency and severity of suicidal thoughts. Minimum score: 0; maximum score: 12.
Time Frame
16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ages 18-24 *The age to provide consent in Nebraska is 19. Individuals recruited from the state of Nebraska must be 19 or older. Current NSSI, defined as self-injury on 2 or more days in the past month Has a smartphone English language skills sufficient to engage in the consent and intervention procedures Exclusion Criteria: Serious mental illness for which intervention would be contraindicated (e.g., psychotic disorder, manic episode, etc.) Severe suicidality (i.e., experiencing suicidal ideation with a plan and intent to act) Current engagement in psychotherapy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kaylee P Kruzan, PhD
Phone
312-503-3114
Email
kaylee.kruzan@northwestern.edu
First Name & Middle Initial & Last Name or Official Title & Degree
David C Mohr, PhD
Phone
312-503-1403
Email
d-mohr@northwestern.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David C Mohr, PhD
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60612
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified data will be shared through and managed by the NIMH Data Archive (NDA). De-identified human subjects data, harmonized to a common standard, are available to qualified researchers.
IPD Sharing Time Frame
Data will be available after publication of the primary outcome papers.
IPD Sharing Access Criteria
The NIMH Data Archive is managed by the NIMH. Access criteria are determined by the NIMH.
IPD Sharing URL
https://nda.nih.gov/

Learn more about this trial

Digital Mental Health Intervention for Nonsuicidal Self-Injury in Young Adults

We'll reach out to this number within 24 hrs