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Behavioral Activation Plus Savoring for University Students

A Randomized Controlled Trial of Behavioral Activation Plus Savoring for University Students With Positive Valence Dysregulation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05234476
Enrollment
60
Registered
2022-02-10
Start date
2021-09-06
Completion date
2022-06-01
Last updated
2022-02-16

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

Conditions

Anhedonia, Depression, Mood

Brief summary

The current investigation aims to examine whether a brief, two-session, virtual behavioral activation plus savoring intervention will increase daily positive emotion in university students.

Detailed description

Experiences of positive emotions are often unchanged following standard psychotherapy. To address this, the current investigation aims to enhance traditional brief behavioral activation with savoring, an emotion regulation strategy specifically targeting positive emotion, or affect, for university students endorsing low levels of the symptom. Individuals will be randomized to either a two-session behavioral activation plus savoring intervention or two sessions of empathic listening. Daily levels of positive emotions will be assessed throughout the study and for one week prior to and completing the intervention.

Interventions

BEHAVIORALBehavioral Activation plus Savoring

Individuals in this intervention will complete two sessions of behavioral activation, where they will be provided psychoeducation on behavioral models of mood, schedule activities, and discuss barriers to completion. Additionally, they will practice savoring as a cognitive strategy to increase positive emotions with a study therapist.

BEHAVIORALEmpathic Listening

Individuals in the active control condition will complete two sessions of reflecting on tracking their mood and empathic listening with a study therapist.

Sponsors

Southern Methodist University
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* University student * Own a smartphone * Positive affect score less than 32 on the Positive and Negative Affect Schedule, Short Form (PANAS-SF)

Design outcomes

Primary

MeasureTime frameDescription
Positive Emotions: Modified Differential Emotions Scale (mDES; Fredrickson et al., 2003)Change from first session to post-treatment (14 days)Positive mood, as measured by the mDES, will be collected two times a day. Participants will be asked to rate their level of positive mood in the moment. Positive mood will be collected on a daily basis throughout the study and change in reported positive emotions will be assessed.

Secondary

MeasureTime frameDescription
Positive and Negative Affect Schedule (PANAS)Change from baseline to post-treatment (21 days)Change in reported symptoms of positive and negative affect following the intervention
Depression, Anxiety, and Stress Scale (DASS-21)Change from baseline to post-treatment (21 days)Change in self-reported symptoms of depression, anxiety, and stress following the intervention

Countries

United States

Contacts

Primary ContactDivya Kumar, M.A.
divyak@smu.edu2147681767

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026