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Mobile Phone Sensing and Outreach as Adjuncts to Internet-Based Behavioral Intervention for Depression

Technology Assisted Intervention for the Treatment and Prevention of Depression

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01107041
Enrollment
2010
Registered
2010-04-20
Start date
2014-12-31
Completion date
2016-07-31
Last updated
2017-03-24

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

Conditions

Depression

Keywords

Depression, Technology Assisted, Mobile Phone

Brief summary

Investigators are evaluating the use of phone sensor data to estimate behavior, depression and anxiety.

Detailed description

Investigators are evaluating the use of phone sensor data to estimate behavior, depression and anxiety. Participants will include people who are high on depression, high on anxiety, hight on both depression and anxiety, and health controls. Particpants will load software on their phones that collects phone sensor data, and obtains self report on sleep, mood, and social contacts. Data will be collected for at least 6 weeks.

Interventions

BEHAVIORALMobilyze!

Mobilyze! delivers behavioral intervention for depression via a mobile phone, interactive website, and e-mail.

Sponsors

Northwestern University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

This study is collecting phone sensor data and ecological momentary assessment data to try to develop algorithms that can passively detect behavioral patterns in participants

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* PHQ-9 score 10 or higher * Has an e-mail account, computer, and broadband access to the Internet * Familiarity with mobile phones and is within a cellular network range the majority of the day. * Is able to speak and read English. * Is at least 19 years of age.

Exclusion criteria

* Hearing or voice impairment preventing participation in psychotherapy. * Visual impairment that would prevent use of the website, mobile phone application, and assessment materials. * Has any psychiatric condition for which participation in a clinical trial of psychotherapy may be either inappropriate or dangerous (e.g., psychotic disorders, bipolar disorders, dissociative disorders, etc.). * Planning to be out of town or unavailable for intervention for 1 or more weeks during the scheduled study participation. * Exhibits severe suicidality, including ideation, plan, and intent.

Design outcomes

Primary

MeasureTime frame
Depression, as assessed the Patient Health Questionnaire-9Baseline, Weeks 2-6

Secondary

MeasureTime frame
Positive Affect (PANAS - Positive Affect Scale)Baseline, Weeks 2-6
Anxiety (GAD-7)Baseline, Weeks 2-6

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026