Skip to content

Skills to Enhance Positive Affect in Suicidal Adolescents

Skills to Enhance Positive Affect in Suicidal Adolescents

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02130583
Acronym
STEP
Enrollment
52
Registered
2014-05-05
Start date
2013-08-31
Completion date
2016-09-02
Last updated
2019-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicidal Ideation, Suicide, Attempted

Brief summary

The prevalence of suicidal behaviors in adolescents remains unacceptably high and is a significant public health concern. The investigators propose a new treatment approach in which skills to increase positive emotions are taught to the most vulnerable at-risk adolescents, those admitted to an inpatient psychiatric unit due to suicide risk. The investigators believe that teaching skills to increase positive emotions will lead to better problem-solving, increased social support, and other benefits which will serve as protective factors and decrease suicide risk.

Detailed description

The prevalence of suicidal behaviors in adolescents remains unacceptably high. Reviews of published randomized controlled trials (RCTs) for adolescent suicidality conclude that treatments to date have been minimally efficacious. The preponderance of interventions focus on crisis intervention, underlying psychiatric disorders, regulating negative affect and reducing cognitive distortions. However, our pilot work and other recent data suggest the importance of considering how low positive affectivity contributes to suicide risk independent of other risk factors and may be another mechanism that leads to suicidal behaviors. Our model is based on Fredrickson's empirically-supported Broaden and Build model which asserts that the function of positive affect (PA) includes helping individuals thrive by improving social supports, problem-solving, and personal resilience. Each of these areas is instrumental in decreasing suicidal behavior. We propose that PA increases survival directly by decreasing suicidal ideation and indirectly by increasing social support and problem-solving. In this R34 treatment development grant we seek to develop a novel, individual skills-based, PA intervention, delivered adjunctively to treatment as usual (TAU), targeting the highest risk adolescents - those hospitalized due to suicide risk. We focus on three strategies that have been demonstrated to increase sustainable (vs. transient) PA in community and depressed adults: meditation, gratitude, and savoring. There are several ways to practice each strategy; we take into account patient preferences in a personalized approach in which patients select the practice(s) that fits best with their needs and circumstances. We propose using multiple means of intervention delivery that includes text messaging, to reinforce in-vivo practice. Our intervention, Skills To Enhance Positivity Program (STEP) includes two phases: a) in-person phase consisting of 3 individual in-person sessions and 1 joint parent session during the inpatient hospital stay to teach positive affect skills and develop a personalized intervention; b) remote delivery phase which consists of weekly telephone booster calls and daily text messages over 4 weeks post-discharge. The phone calls will be used to review or adjust personalized intervention components and reinforce use of skills. The text messages will include self-scripted reminders to practice skills and links to online resources. STEP will be tested in an open trial with 20 participants, and after further revision, in a pilot RCT, compared to TAU in a sample of 50 adolescents. The primary goal of this intervention is for patients to increase positive affect by incorporating skills and practices into their normal home-based routines, which we believe will lead to increases in problem-solving and social support and decreases in suicidal ideation. This is a novel intervention for a high-risk acute population via a different mechanism (i.e. PA), and conceptually distinct from other empirically examined theoretical approaches.

Interventions

Individual sessions (3-4) delivered on the inpatient unit, focused on psycho-education regarding positive affect and mood monitoring and teaching of skills to attend to positive affect such as mindfulness, gratitude, and savoring. In-person sessions are followed by weekly phone calls and daily text messages for one month, with option to extend.

BEHAVIORALTreatment as Usual

Participants will follow the intervention plan laid out in their discharge summary, but do not receive any individual sessions regarding positive affect. Upon discharge, they will receive generic text messages regarding healthy habits for one month, with option to extend.

Sponsors

Brown University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* current hospital admission due to concern of suicide risk * ability of patient to speak, read, and understand English sufficiently well to complete the procedures of the study * living at home

Exclusion criteria

* active psychotic disorder * cognitive deficits that preclude full understanding of study materials * adolescents who have become wards of the state and do not intend to return to the home of their biological or adoptive parents

Design outcomes

Primary

MeasureTime frameDescription
Suicide Events1 month, 6 monthNumber of participants who have attempted suicide or have had emergency intervention to intercede a suicide attempt.
Dot Probe TaskBaseline, 1 month Post Treatment, 4 month Follow-UpDot probe tasks are administered to assess for attentional biases. The task is a computer task in which participants are presented with stimuli (e.g., words) of different valences (positive/negative/neutral) at the same time (e.g., smiling face and a neutral face), followed by a probe (\*) on one side. Participants are asked to hit a key that corresponds to the correct side in which the probe appeared. The reaction time of their response is indicative of their attention to the valenced image/word. Trials are counterbalanced so that valences appear equally on each side. Faster reaction time (less milliseconds) to positive images/words indicates an attentional bias for positive stimuli. The scores reported here represent bias scores. Positive scores indicate a bias to positive stimuli, negative scores indicate a bias towards neutral stimuli.
Modified Differential Emotions Scale (Positive Emotions Sub-scale)Base, 1 month Post-Treatment, 4 month Follow-UpThe Modified Differential Emotions Scale is a self-report measure comprised of ratings for positive and negative affect. For example, participants are asked to rate the extent to which they feel Content, serene, peaceful right now on a likert scale ranging from 1 (not at all) to 5 (extremely). The scores reported are averages for the positive emotions, and thus can be interpreted as ranging from 1 (not at all) to 5 (extremely). We expected an increase in positive affect ratings following the intervention.

Secondary

MeasureTime frameDescription
Columbia Impairment Scale Parent VersionBase, 1 month Post-Treatment, 4 month Follow-UpThe Columbia Impairment Scale (parent version) is a 13-item scale in which parents are asked to respond about their child's impairment in a variety of domains on a scale of 0 (no problem at all) to 4 (very bad problem). Scores are summed such that higher scored indicate higher functional impairment, with a maximum score of 52 and a minimum score of 0.
Suicide Ideation Questionnaire (SIQ)Baseline, 1 month Post-Treatment, 4 month Follow-UpThe Suicidal Ideation Questionnaire is a 30 item self-report measure that was administered to the adolescent to ascertain the frequency of thoughts of death and suicide. Respondents are asked how often they have had these thoughts (e.g., I thought about killing myself) in the past month ranging from almost every day = 1 to I never had this thought =7. Scores are then reversed and transformed such that higher scores indicate higher suicidal ideation, with a range of 180 (highest suicidal ideation) to 0 (no suicidal ideation).
Beck Depression InventoryBaseline, 1 month Post-Treatment, 4 month Follow-UpThe Beck Depression Inventory is a 21 item self-report form of depression but can be and has been administered to the parent to respond about their child. This questionnaire consists of 21 groups of statements. For example, for Sadness, respondents are asked to select between 0 (My child does not feel sad.), 1 (My child feels sad much of the time), 2 (My child is sad all the time), and 3 (My child is so sad or unhappy that he/she can't stand it.). Higher scores indicate higher depression with a maximum score of 63 and a minimum score of 0.

Other

MeasureTime frameDescription
Hopelessness Scale for ChildrenBaseline, 1 month Post-Treatment, 4 month Follow-UpThe Hopelessness Scale for Children is a 17 item self-report scale with statements (e.g., I want to grow up because I think things will be better) that are rated as either True or False. Some statements are reverse coded. Higher scores indicate higher hopelessness, with a maximum score of 17 and a minimum score of 0.

Countries

United States

Participant flow

Recruitment details

Participants in this study were adolescents who were hospitalized at a psychiatric hospital in Rhode Island due to concern of suicide risk. The last participant completed the study procedures in September 2016.

Participants by arm

ArmCount
Positive Affect Skills Training
Individual sessions (3-4) delivered on the inpatient unit, focused on psycho-education regarding positive affect and mood monitoring and teaching of skills to attend to positive affect such as mindfulness, gratitude, and savoring. In-person sessions are followed by weekly phone calls and daily text messages for one month, with option to extend. Positive Affect Skills Training: Individual sessions (3-4) delivered on the inpatient unit, focused on psycho-education regarding positive affect and mood monitoring and teaching of skills to attend to positive affect such as mindfulness, gratitude, and savoring. In-person sessions are followed by weekly phone calls and daily text messages for one month, with option to extend.
26
Treatment as Usual
Participants will follow the intervention plan laid out in their discharge summary, but do not receive any individual sessions regarding positive affect. Upon discharge, they will receive generic text messages regarding healthy habits for one month, with option to extend. Treatment as Usual: Participants will follow the intervention plan laid out in their discharge summary, but do not receive any individual sessions regarding positive affect. Upon discharge, they will receive generic text messages regarding healthy habits for one month, with option to extend.
26
Total52

Baseline characteristics

CharacteristicPositive Affect Skills TrainingTreatment as UsualTotal
Age, Continuous15.69 years
STANDARD_DEVIATION 1.1715
15.58 years
STANDARD_DEVIATION 1.206
15.63 years
STANDARD_DEVIATION 1.469
Ethnicity (NIH/OMB)
Hispanic or Latino
6 Participants7 Participants13 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
20 Participants19 Participants39 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Sex: Female, Male
Female
18 Participants18 Participants36 Participants
Sex: Female, Male
Male
8 Participants8 Participants16 Participants
Sex/Gender, Customized
Female
15 Participants17 Participants32 Participants
Sex/Gender, Customized
Male
10 Participants9 Participants19 Participants
Sex/Gender, Customized
Other
1 Participants0 Participants1 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 260 / 26
other
Total, other adverse events
0 / 260 / 26
serious
Total, serious adverse events
5 / 2612 / 26

Outcome results

Primary

Dot Probe Task

Dot probe tasks are administered to assess for attentional biases. The task is a computer task in which participants are presented with stimuli (e.g., words) of different valences (positive/negative/neutral) at the same time (e.g., smiling face and a neutral face), followed by a probe (\*) on one side. Participants are asked to hit a key that corresponds to the correct side in which the probe appeared. The reaction time of their response is indicative of their attention to the valenced image/word. Trials are counterbalanced so that valences appear equally on each side. Faster reaction time (less milliseconds) to positive images/words indicates an attentional bias for positive stimuli. The scores reported here represent bias scores. Positive scores indicate a bias to positive stimuli, negative scores indicate a bias towards neutral stimuli.

Time frame: Baseline, 1 month Post Treatment, 4 month Follow-Up

Population: Numbers may differ due to participant attrition and invalid profiles.

ArmMeasureGroupValue (MEAN)Dispersion
STEPDot Probe TaskBaseline1.56 millisecondsStandard Deviation 18.12
STEPDot Probe TaskPost-Treatment-1.48 millisecondsStandard Deviation 13.85
STEPDot Probe TaskFollow-up6.88 millisecondsStandard Deviation 34.12
ETAUDot Probe TaskBaseline-1.65 millisecondsStandard Deviation 17.43
ETAUDot Probe TaskPost-Treatment1.23 millisecondsStandard Deviation 18.75
ETAUDot Probe TaskFollow-up-19.8 millisecondsStandard Deviation 40.36
p-value: 0.034ANOVA
Primary

Modified Differential Emotions Scale (Positive Emotions Sub-scale)

The Modified Differential Emotions Scale is a self-report measure comprised of ratings for positive and negative affect. For example, participants are asked to rate the extent to which they feel Content, serene, peaceful right now on a likert scale ranging from 1 (not at all) to 5 (extremely). The scores reported are averages for the positive emotions, and thus can be interpreted as ranging from 1 (not at all) to 5 (extremely). We expected an increase in positive affect ratings following the intervention.

Time frame: Base, 1 month Post-Treatment, 4 month Follow-Up

Population: Some participants were lost to follow-up.

ArmMeasureGroupValue (MEAN)Dispersion
STEPModified Differential Emotions Scale (Positive Emotions Sub-scale)Baseline1.97 units on a scaleStandard Deviation 0.71
STEPModified Differential Emotions Scale (Positive Emotions Sub-scale)Post-Treatment1.95 units on a scaleStandard Deviation 0.62
STEPModified Differential Emotions Scale (Positive Emotions Sub-scale)Follow-up1.98 units on a scaleStandard Deviation 0.82
ETAUModified Differential Emotions Scale (Positive Emotions Sub-scale)Baseline2.09 units on a scaleStandard Deviation 0.71
ETAUModified Differential Emotions Scale (Positive Emotions Sub-scale)Post-Treatment2.26 units on a scaleStandard Deviation 0.97
ETAUModified Differential Emotions Scale (Positive Emotions Sub-scale)Follow-up2.06 units on a scaleStandard Deviation 0.87
Primary

Suicide Events

Number of participants who have attempted suicide or have had emergency intervention to intercede a suicide attempt.

Time frame: 1 month, 6 month

Population: Some participants were lost to follow-up

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
STEPSuicide EventsPost-Treatment2 Participants
STEPSuicide Events6 Month Follow Up5 Participants
ETAUSuicide Events6 Month Follow Up10 Participants
ETAUSuicide EventsPost-Treatment7 Participants
Secondary

Beck Depression Inventory

The Beck Depression Inventory is a 21 item self-report form of depression but can be and has been administered to the parent to respond about their child. This questionnaire consists of 21 groups of statements. For example, for Sadness, respondents are asked to select between 0 (My child does not feel sad.), 1 (My child feels sad much of the time), 2 (My child is sad all the time), and 3 (My child is so sad or unhappy that he/she can't stand it.). Higher scores indicate higher depression with a maximum score of 63 and a minimum score of 0.

Time frame: Baseline, 1 month Post-Treatment, 4 month Follow-Up

Population: Some participants' parents did not participate (e.g. if teen was = 18 y/o); Also, some parents were lost to follow-up.

ArmMeasureGroupValue (MEAN)Dispersion
STEPBeck Depression InventoryBaseline27.88 units on a scaleStandard Deviation 25.79
STEPBeck Depression InventoryPost-treatment11.56 units on a scaleStandard Deviation 11.35
STEPBeck Depression InventoryFollow-Up11.88 units on a scaleStandard Deviation 10.9
ETAUBeck Depression InventoryBaseline29.77 units on a scaleStandard Deviation 8.18
ETAUBeck Depression InventoryPost-treatment20.70 units on a scaleStandard Deviation 11.73
ETAUBeck Depression InventoryFollow-Up16.83 units on a scaleStandard Deviation 12.66
Secondary

Columbia Impairment Scale Parent Version

The Columbia Impairment Scale (parent version) is a 13-item scale in which parents are asked to respond about their child's impairment in a variety of domains on a scale of 0 (no problem at all) to 4 (very bad problem). Scores are summed such that higher scored indicate higher functional impairment, with a maximum score of 52 and a minimum score of 0.

Time frame: Base, 1 month Post-Treatment, 4 month Follow-Up

Population: Some participants' parents did not participate (e.g. if teen was = 18 y/o); Also, some parents were lost to follow-up.

ArmMeasureGroupValue (MEAN)Dispersion
STEPColumbia Impairment Scale Parent VersionBaseline25.79 units on a scaleStandard Deviation 10.14
STEPColumbia Impairment Scale Parent VersionPost-treatment17.33 units on a scaleStandard Deviation 10.21
STEPColumbia Impairment Scale Parent VersionFollow-Up13.82 units on a scaleStandard Deviation 7.23
ETAUColumbia Impairment Scale Parent VersionBaseline26.68 units on a scaleStandard Deviation 9.17
ETAUColumbia Impairment Scale Parent VersionPost-treatment21.43 units on a scaleStandard Deviation 10.59
ETAUColumbia Impairment Scale Parent VersionFollow-Up19.78 units on a scaleStandard Deviation 8.91
Secondary

Suicide Ideation Questionnaire (SIQ)

The Suicidal Ideation Questionnaire is a 30 item self-report measure that was administered to the adolescent to ascertain the frequency of thoughts of death and suicide. Respondents are asked how often they have had these thoughts (e.g., I thought about killing myself) in the past month ranging from almost every day = 1 to I never had this thought =7. Scores are then reversed and transformed such that higher scores indicate higher suicidal ideation, with a range of 180 (highest suicidal ideation) to 0 (no suicidal ideation).

Time frame: Baseline, 1 month Post-Treatment, 4 month Follow-Up

Population: Some participants were lost to follow up.

ArmMeasureGroupValue (MEAN)Dispersion
STEPSuicide Ideation Questionnaire (SIQ)Baseline100.04 units on a scaleStandard Deviation 44.42
STEPSuicide Ideation Questionnaire (SIQ)Post-Treatment51.71 units on a scaleStandard Deviation 55.24
STEPSuicide Ideation Questionnaire (SIQ)Follow-up47.81 units on a scaleStandard Deviation 52.96
ETAUSuicide Ideation Questionnaire (SIQ)Baseline106.00 units on a scaleStandard Deviation 40.28
ETAUSuicide Ideation Questionnaire (SIQ)Post-Treatment70.96 units on a scaleStandard Deviation 42.72
ETAUSuicide Ideation Questionnaire (SIQ)Follow-up43.24 units on a scaleStandard Deviation 45.66
Other Pre-specified

Hopelessness Scale for Children

The Hopelessness Scale for Children is a 17 item self-report scale with statements (e.g., I want to grow up because I think things will be better) that are rated as either True or False. Some statements are reverse coded. Higher scores indicate higher hopelessness, with a maximum score of 17 and a minimum score of 0.

Time frame: Baseline, 1 month Post-Treatment, 4 month Follow-Up

Population: Some participants were lost to follow up.

ArmMeasureGroupValue (MEAN)Dispersion
STEPHopelessness Scale for ChildrenFollow-up9.71 units on a scaleStandard Deviation 5.98
STEPHopelessness Scale for ChildrenBaseline7.35 units on a scaleStandard Deviation 5.26
STEPHopelessness Scale for ChildrenPost-Treatment9.24 units on a scaleStandard Deviation 5.96
ETAUHopelessness Scale for ChildrenBaseline7.77 units on a scaleStandard Deviation 5
ETAUHopelessness Scale for ChildrenPost-Treatment10.58 units on a scaleStandard Deviation 4.67
ETAUHopelessness Scale for ChildrenFollow-up11.67 units on a scaleStandard Deviation 5.69

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026