Behavioral Activation Plus Savoring for University Students

Sponsor
Southern Methodist University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05234476
Collaborator
(none)
60
1
2
8.8
6.8

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Behavioral Activation plus Savoring
  • Behavioral: Empathic Listening
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
A Randomized Controlled Trial of Behavioral Activation Plus Savoring for University Students With Positive Valence Dysregulation
Actual Study Start Date :
Sep 6, 2021
Anticipated Primary Completion Date :
Jun 1, 2022
Anticipated Study Completion Date :
Jun 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Behavioral 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.

Behavioral: Behavioral 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.

Active Comparator: Empathic Listening

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

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

Outcome Measures

Primary Outcome Measures

  1. 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 Outcome Measures

  1. 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

  2. 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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Southern Methodist University Dallas Texas United States 75206

Sponsors and Collaborators

  • Southern Methodist University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Southern Methodist University
ClinicalTrials.gov Identifier:
NCT05234476
Other Study ID Numbers:
  • 21-118
First Posted:
Feb 10, 2022
Last Update Posted:
Feb 16, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 16, 2022