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The Effect of a Brief Online Behavioral Activation Intervention

The Effect of a Brief Online Behavioral Activation Intervention by Activity Type

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05914025
Enrollment
106
Registered
2023-06-22
Start date
2022-01-24
Completion date
2023-04-18
Last updated
2023-06-22

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

Conditions

Depression

Brief summary

Depression is a worldwide phenomena that has a severe personal, social and societal impact. One such impact is an over $200 billion worldwide economic cost. While many treatments exist for depression, many individuals may not receive the support that they need for reasons such as stigma, financial restraints, or limited access to therapists. As such, it is important to assess the efficacy of brief online treatments as an alternative to full length, in-person treatments. A series of studies looking at a brief behavioral activation for depression treatment has shown that participants have reported temporarily improved mood, confidence, motivation and reduced depressive symptoms. It is important to test this treatment in multiple groups of people to acquire additional information regarding brief online interventions. This study seeks to collect participants from online social media sources and compare results to historical data that were collected from a prior research study which used Amazon Mechanical Turk as a recruitment source.

Interventions

BEHAVIORALBehavioral Activation

Individuals will be provided with information about maladaptive patterns of behavior and how to correct these cycles with activity scheduling to elicit more positive emotional experiences. Participants will be provided with categories/lists of activities and a downloadable calendar after receiving the psychoeducation.

Sponsors

Palo Alto University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 18 years of age or older * United States Resident

Exclusion criteria

* Non-US resident * Younger than 18 years old

Design outcomes

Primary

MeasureTime frameDescription
Depression level3 daysChanges in depression score as measured by the PROMIS scale. The PROMIS is scored on a 5-point Likert scale with responses 1 to 5 corresponding to Never, Rarely, Sometimes, Often, and Always respectively.
Self-reported mood3 daysChanges in mood as measured by a self-reported mood question. This measure is scored on a 9-point Likert scale (1 = Extremely Negative to 9 = Extremely Positive)
Daily EnjoymentAt time of original surveyChanges in enjoyment as measured by a self-reported question around daily enjoyment. This measure is scored on a 5-point Likert scale (1 = Not at all to 9 = Extremely)

Secondary

MeasureTime frameDescription
Confidence, Motivation, and Usefulness3 daysChanges in confidence, motivation, and usefulness are measured with single self-reported measures for confidence, motivation, and usefulness of the intervention. They are rated on a 9 point Likert scale (1 = Extremely Negative to 9 = Extremely Positive)

Countries

United States

Outcome results

None listed

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