What SSI Duration is Most Effective? An Online Experiment With American Adults

NCT06313736 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1145

Last updated 2024-09-19

No results posted yet for this study

Summary

In a previous study (https://osf.io/qdznc), the research team found that an 8-minute version of a single-session intervention for loneliness was more effective than a 23-minute version of it. The present work aims to further explore the relationship between intervention duration and effectiveness.

In this online trial, participants will be randomized to a 15-minute single-session depression intervention called the Action Brings Change (ABC) Program, a 10-minute version of it, a 6-minute version of it, or a 2-minute version of it. The main analysis will evaluate how change in depressive symptoms over eight weeks differs across conditions.

Conditions

Interventions

BEHAVIORAL

Action Brings Change Project (15-minute adult version)

The ABC Project is a self-guided online single-session intervention based on principles of behavioral activation. In a slightly different form intended for adolescents, it has demonstrated efficacy in several studies. Its adult version has also shown some efficacy.

BEHAVIORAL

Action Brings Change Project (10-minute adult version)

This is a 10-minute shortened version of the 15-minute adult version of the ABC Project. The research team created it and pilot-tested it.

BEHAVIORAL

Action Brings Change Project (6-minute adult version)

This is a 6-minute shortened version of the 15-minute adult version of the ABC Project. The research team created it and pilot-tested it.

BEHAVIORAL

Action Brings Change Project (2-minute adult version)

This is a 2-minute shortened version of the 15-minute adult version of the ABC Project. The research team created it and pilot-tested it.

Sponsors & Collaborators

Principal Investigators

  • Jessica L Schleider, PhD · Northwestern University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-03-20
Primary Completion
2024-05-22
Completion
2024-05-22

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06313736 on ClinicalTrials.gov