CClinicalTrials.gg
Not yet recruitingNCT07593443Updated May 18, 2026

Application for Arts-Based Social Prescribing

An interventional study of Art Pharmacy and Stable treatment in Depression in Adolescence, Anxiety and Loneliness, sponsored by SocialRx Inc. Not yet recruiting. Open to participants aged 15 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-05-18.

Sponsored by SocialRx Inc · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
230
Allocation
Randomized
Ages
15 Years to 18 Years
Sex
All
01

Study summary

The goal of this clinical trial is to learn if a personalized arts-based social prescribing program, Art Pharmacy, delivered through a mobile app (SocialRx App) can improve mental health and social connectedness in adolescents aged 15-18 with depression or anxiety enrolled in Medicaid managed care.

The main question it aims to answer is:

Compared to stable treatment, does participation in the Art Pharmacy program through the SocialRx App improve depression, anxiety, social connectedness, and loneliness? Researchers will compare participants receiving the Art Pharmacy program and digital companion to those receiving stable treatment (no change to existing care) to evaluate its effects on mental health and social connectedness.

Participants will:

Be randomly assigned to either the Art Pharmacy program delivered through the SocialRx App or a control group receiving stable treatment.

Complete online surveys at baseline and follow-up time points (e.g., 3, 6, 9, and 12 months).

If assigned to the intervention group, Art Pharmacy, participants will receive monthly arts and cultural activity recommendations, attend activities, and interact with a care navigator delivered through the SocialRx App.

02

Conditions studied

  • Depression in Adolescence
  • Anxiety
  • Loneliness
  • Social Connectedness

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03

In context

Anxiety Disorders

4,868 studies on the registry are indexed under Anxiety Disorders; 1,390 are open to participants now.

This study's planned enrollment of 230 is above the median of 80 across 4,174 interventional studies indexed under Anxiety Disorders.

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Lead sponsor

This is the only study on the registry with SocialRx Inc as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
15 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Participants must meet the following criteria:

  • Aged 15-18 years enrolled in Medicaid managed care
  • Positive screen for depression and/or anxiety (e.g., PHQ-2 or GAD-2 ≥ 3)
  • Currently own and easily operate a smartphone
  • Have a valid e-mail address checked regularly
  • English fluency, and
  • Have a stable treatment regimen for at least 30 days prior to baseline with no planned treatment changes.

Exclusion criteria

Exclusion Criteria:

Participants will be excluded if they:

  • Endorse current suicidal ideation at study screening, defined as a response ≥ 1 ("several days") on Item 9 of the PHQ-9A
  • Initiate a new treatment regimen or plan on initiating a new treatment regimen (i.e., medication, psychotherapy, or mind-body interventions) at the time of enrollment.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
230 participants (estimated)

Study arms

  • Experimental
    Art Pharmacy program delivered through the SocialRx App

    A personalized arts-based social prescribing program, Art Pharmacy, delivered through a mobile app, SocialRx App

    Behavioral: Art Pharmacy

  • Active comparator
    Stable treatment

    Existing, stable treatment regimen without major changes

    Other: Stable treatment

Interventions

  • BehavioralArt Pharmacy

    A personalized arts-based social prescribing program

  • OtherStable treatment

    Stable treatment (no change to existing care) through Medicaid managed care

06

What researchers measure

Primary outcomes

  1. Anxiety - Generalized Anxiety Disorder-7 (GAD-7)

    The GAD-7 is a 7-item self-report measure of anxiety symptoms. Scores range from 0 to 21, with higher scores indicating greater anxiety severity.

    Time frame: At baseline, and 3-, 6-, 9- and 12-month follow up.

  2. Depression - Patient Health Questionnaire-9 Adolescent Version (PHQ-9A)

    The PHQ-9A is a 9-item self-report measure of depressive symptoms in adolescents. Scores range from 0 to 27, with higher scores indicating greater depression severity.

    Time frame: At baseline, and 3-, 6-, 9- and 12-month follow up.

  3. Loneliness - UCLA Loneliness Scale

    The UCLA Loneliness Scale assesses subjective feelings of loneliness and social isolation. Scores range from 20 - 80, with higher scores indicating a higher degree of loneliness.

    Time frame: At baseline, and 3-, 6-, 9-, and 12-month follow up

  4. Social Connectedness - Social Connectedness Scale-Revised (SCS-R)

    The SCS-R measures feelings of interpersonal closeness and connectedness. Scores range from 20 to 120, with higher scores indicating greater social connectedness.

    Time frame: At baseline, and 3-, 6-, 9-, and 12-month follow up

Secondary outcomes

  1. Treatment Utilization - Treatment and Arts/Cultural Engagement Utilization Questionnaire

    A study-developed questionnaire assessing participant engagement with behavioral health treatment and arts/cultural activities. Higher scores/frequencies indicate greater utilization and engagement.

    Time frame: At baseline, and 3-, 6-, 9-, and 12-month follow up

07

Study locations

No study locations are listed for this record.

08

References and documents

Study documents

  • Protocol and statistical analysis plan · May 13, 2026

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 18, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07593443
Lead sponsor
SocialRx Inc
Collaborators
National Center for Complementary and Integrative Health (NCCIH), Boston College
Responsible party
Dawn McDaniel (Research Scientist, SocialRx Inc) — Principal investigator
First posted
May 18, 2026
Start date
May 2026 (estimated)
Primary completion
Jan 2028 (estimated)
Completion
Apr 2028 (estimated)
Last update
May 18, 2026

Study contacts

Peter Research & Evaluation Manager
Contact
peter@socialrx.com
845-807-8005
Dawn McDaniel, PhD
principal investigator · SocialRx Inc

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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