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Brief Mood Enhancement Intervention

Enhancing Mood Among Graduate Students: Evaluation of a Brief, Phone-Administered Behavioral Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02954965
Enrollment
66
Registered
2016-11-04
Start date
2016-11-30
Completion date
2017-12-31
Last updated
2018-02-23

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

Conditions

Stress, Psychological, Burnout, Professional

Keywords

graduate student, burnout, stress, mood

Brief summary

The purpose of the current study is to test the efficacy of two brief, behavioral interventions intended to improve burnout among doctoral-level graduate students (n = 102). Specifically, individuals will be randomly assigned to one of three intervention conditions: 1) Reward: a brief intervention to help participants increase engagement in healthy and rewarding values-driven behaviors, 2) Approach: a brief intervention to help participants identify and decrease emotion-driven avoidance of important goals, or 3) Control: a control condition that involves monitoring only. Multilevel modeling will be used to assess changes in burnout, mood, and stress, following the interventions, controlling for participants' individual baseline levels of these variables.

Interventions

BEHAVIORALReward

Brief behavioral intervention (administered during a 45-minute phone call) that is designed to improve graduate student burnout by helping participants to identify activities that are rewarding and pleasurable and to integrate these activities into their schedule.

BEHAVIORALApproach

Brief behavioral intervention (administered during a 45-minute phone call) that is designed to improve graduate student burnout by helping participants to identify activities that are challenging, but important to their long-term goals and values, and to integrate these activities into their schedule.

Sponsors

Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Currently enrolled in any in-person (not online) Ph.D. program in the state of North Carolina * Demonstrating above average levels of burnout * Has regular access to the Internet * Has a Social Security Number * Is able to read and understand English

Exclusion criteria

* Current mania or psychosis * Current suicidal ideation * Are currently in psychotherapy, have been in psychotherapy in the past 8 weeks, or are planning to start psychotherapy during the course of the 10-day study * Have had any changes in psychiatric medications in the past 8 weeks, are not taking medications as prescribed or are planning to change medications during the course of the 10-day study * Are currently taking benzodiazepines Pro Re Nata (PRN) * Are under 18 years old

Design outcomes

Primary

MeasureTime frameDescription
Change in burnout, as measured by the School Burnout Inventory total scorebaseline (day 0) and post-intervention (day 10)Self-report questionnaire assessing burnout
Change in stress, as measured by the Perceived Stress Scale total scorebaseline (day 0) and post-intervention (day 10)Self-report questionnaire assessing stress

Secondary

MeasureTime frameDescription
Change in mood, as measured by the Positive and Negative Affect Schedule total scores for Positive and Negative Affectbaseline (day 0) and post-intervention (day 10)Self-report questionnaire assessing mood
Change in reward, as measured by the Environmental Reward Observation Scale total scorebaseline (day 0) and post-intervention (day 10)Self-report questionnaires assessing environmental reward
Change in behavioral activation, as measured by the Activation sub-scale of the Behavioral Activation for Depression Scalebaseline (day 0) and post-intervention (day 10)Self-report questionnaires assessing behavioral activation
Change in functional impairment, as measured by the Modified Work and Social Adjustment Scale total scorebaseline (day 0) and post-intervention (day 10)Self-report questionnaire assessing functional impairment
Change in mastery, as measured by the Pearlin Personal Mastery Scale total scorebaseline (day 0) and post-intervention (day 10)Self-report questionnaires assessing mastery
Change in depression symptoms, as measured by the General Depression scale of the Inventory of Depression and Anxiety Symptomsbaseline (day 0) and post-intervention (day 10)Self-report questionnaire assessing depression symptoms
Change in mastery, as measured by the average of the daily Importance ratings of activities (0-10) on the Daily Activities Monitoring Formbaseline (days 0-3) and intervention (days 3-10)Self-report monitoring form describing activities during the day, how enjoyable they were, and how important they were
Change in avoidance, as measured by the total score of the Avoidance/Rumination sub-scale of the Behavioral Activation for Depression Scalebaseline (day 0) and post-intervention (day 10)Self-report questionnaire assessing avoidance and rumination
Change in environmental reward, as measured by the average of the daily Pleasure ratings of activities (0-10) on the Daily Activities Monitoring Formbaseline (days 0-3) and intervention (days 3-10)Self-report monitoring form describing activities during the day, how enjoyable they were, and how important they were
Change in quality of life, as measured by the WHOQOL-BREF total scorebaseline (day 0) and post-intervention (day 10)Self-report questionnaire assessing quality of life
Change in avoidance, as measured by the Brief Experiential Avoidance Questionnaire total scorebaseline (day 0) and post-intervention (day 10)Self-report questionnaires assessing avoidance

Countries

United States

Outcome results

None listed

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