Skip to main content
Clinical Trials/NCT03816215
NCT03816215CompletedNot Applicable

Volunteering as an Intervention to Reduce Depression Among Adolescents: Investigating Neurobiological Mechanisms

Wake Forest University Health Sciences3 sites in 1 country9 target enrollmentStarted: June 3, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
9
Locations
3
Primary Endpoint
Participant recruitment

Study Overview

Brief Summary

The purpose of the present study is to test in a preliminary manner an innovative strategy for treating depression among adolescents (alongside existing therapy) using community volunteerism.

Detailed Description

The purpose of the present study is to test in a preliminary manner an innovative strategy for treating depression among adolescents (alongside existing therapy) using community volunteerism. In addition, this study will test a potential mechanism by which volunteering might decrease depressive symptoms: increasing psychosocial assets, specifically decreasing self-orientation and increasing an orientation toward others. This will be measured through self-report as well as using functional magnetic resonance imaging (fMRI). This study will be the first study to explore how neural response patterns are potentially altered by intense experiences with volunteerism among depressed adolescents.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
14 Years to 20 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •age 14-20
  • •new mild to moderate depression diagnosis (single episode)
  • •new mild to moderate anxiety diagnosis
  • •new adjustment disorder diagnosis
  • •have been in treatment for < 8 months
  • •right-handed

Exclusion Criteria

  • •history of recurrent depressive, anxiety or adjustment disorder episodes
  • •have been in treatment > 8 months
  • •left-handed
  • •expressing suicidal ideation
  • •claustrophobia
  • •any contraindications for completing an MRI scan

Arms & Interventions

Adolescent Participants

Experimental

Participants will be assigned to participate in community service (from a menu of options) for 30 hours.

Intervention: Volunteer experience (Behavioral)

Outcomes

Primary Outcomes

Participant recruitment

Time Frame: 6 months

Number of participants screened (reported by clinical mental health providers)

Participant retention

Time Frame: 6 months

Number of participants retained in full study

Depressive symptoms (Beck Depression Inventory)

Time Frame: 6 months

Beck Depression Inventory to measure depressive symptoms. Each item is rated on a 4-point scale ranging from 0 to 3. The minimum total score is 0 and the maximum total score is 63. Higher scores denote worse outcome

Secondary Outcomes

  • Self-efficacy(6 months)
  • Empathy(6 months)
  • Strength of Connectivity in DMN (Default Mode Network)(6 months)
  • Hope scale (Abler et al., 2017)(6 months)
  • Beck Hopelessness Inventory(6 months)
  • Orientation Toward Others(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (3)

Loading locations...

Similar Trials