Volunteer experience
BehavioralParticipants will be assigned to a meaningful volunteer experience from a menu of local options (e.g., volunteering at an animal shelter or in a library) for 30 hours.
NCT Number: NCT03816215
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.
Looking for future studies?
Notify Me14 year–20 year
All sexes
Interventional
Not applicable
Private practice, Winston-Salem, North Carolina, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will be assigned to a meaningful volunteer experience from a menu of local options (e.g., volunteering at an animal shelter or in a library) for 30 hours.
Time frame: 6 months
Number of participants screened (reported by clinical mental health providers)
Time frame: 6 months
Number of participants retained in full study
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
Time frame: 6 months
Default Mode Network Connectivity will be measured using fMRI at rest and while processing emotional pictures before and after volunteering intervention. The strength of connectivity within the DMN will be calculated by averaging attributes for each node in the DMN.
Time frame: 6 months
Hope scale (Abler et al., 2017) will be measured on a scale from 1 (strongly disagree) to 5 (strongly agree). Items will be averaged; higher scores denote better outcome (more hope).
Time frame: 6 months
Beck Hopelessness Inventory will be used (scored from 1-20; higher score denotes worse outcome).
Time frame: 6 months
NIH toolbox measure from 1 (never) to 5 (very often); scores will be averaged and high score indicates more self-efficacy.
Time frame: 6 months
5 point scale from 1=strongly disagree to 5=strongly agree. Scores will be averaged; higher score denotes more orientation toward others.
Time frame: 6 months
IRI (Interpersonal Reactivity Index) subscale to measure empathy on a 5 point scale from 1- strongly disagree to 5 -strongly agree. Scores will be averaged; higher score denotes more empathy.
Time frame: 6 months
Measured through the Inventory of Service Experience (Taylor & Pancer, 2007) on a scale from 1 (strongly disagree) to 5 (strongly agree). Scores will be averaged for subscales of the measure. Higher score denotes better outcomes (more positive experiences with volunteering).
Wake Forest University Health Sciences
Other
Volunteering as an Intervention to Reduce Depression Among Adolescents: Investigating Neurobiological Mechanisms
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04951193
Adolescent Behavior, Behavior
Charleston, South Carolina, United States
View Trial DetailsNCT06173544
Adolescent Behavior, Anxiety
Lilongwe, Malawi
View Trial DetailsNCT05476237
Adolescent Behavior, Behavior
Maputo, Mozambique
View Trial DetailsNCT06083987
Adolescent Behavior, Anxiety
Pittsburgh, Pennsylvania, United States
View Trial Details