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Skills to Enhance Positivity in Young Adults

Skills to Enhance Positivity in Young Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06621992
Acronym
STEP YA
Enrollment
53
Registered
2024-10-01
Start date
2016-12-31
Completion date
2019-07-31
Last updated
2024-10-01

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

Conditions

Depression, Gratitude, Mindfulness, Positive Affect, Savoring

Brief summary

The goal of this study is to test the feasibility and acceptability of a positive affect intervention for suicide in a population of young adults. Skills to Enhance Positivity (STEP) has been demonstrated to be feasible and acceptable among adolescents when delivered individually. The current study aims to test feasibility and acceptability in a group setting of young adults. The specific aims of STEP also seek to establish whether participants who received STEP report a significant increase in attention towards positive affect compared to those receiving Treatment As Usual (TAU). They also seek to explore whether participants who received STEP will report a significant decrease in suicidal ideation and depression compared to those receiving TAU. The final aim is to explore whether an increase in attention to positive affect regardless of condition is a potential mechanism of change for reductions in suicidal ideation and depression. Participants will be randomized into STEP or TAU groups, they will complete baseline and follow-up assessments after a period of 3-months. Participants enrolled in STEP will receive in-person group sessions focusing on psychoeducation of positive affect as well as skills in mindfulness, gratitude and savoring designed to promote positive affect. After completing the group sessions they will also receive text messages for one month, where they will receive prompts to practice skills they learned in the group setting.

Interventions

OTHERSkills to Enhance Positivity
OTHERTreatment as Usual

Participants received treatment as usual

Sponsors

Rhode Island Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 26 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants must have a recent history of depression and are English-speaking * Participants also must have a cell phone with text-messaging capabilities

Exclusion criteria

* Participants who have acute psychotic disorders or cognitive deficits that would preclude full understanding of the protocol, intervention and assessment materials

Design outcomes

Primary

MeasureTime frameDescription
Feasibility and Acceptability of a group interventionWill be assessed at follow-up at 3-monthsFeasibility and acceptability will be evaluated using self-report questionnaires and interviews

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 21, 2026