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OpenTrials
Completed

NCT Number: NCT01107041

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

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

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Northwestern University

Chicago, Illinois, 60611, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Mobilyze!

Behavioral

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

Primary outcomes

  1. Depression, as assessed the Patient Health Questionnaire-9

    Time frame: Baseline, Weeks 2-6

Secondary outcomes

  1. Positive Affect (PANAS - Positive Affect Scale)

    Time frame: Baseline, Weeks 2-6

  2. Anxiety (GAD-7)

    Time frame: Baseline, Weeks 2-6

Sponsors and collaborators

Lead sponsor

Northwestern University

Other

Registry information

Official study title

Technology Assisted Intervention for the Treatment and Prevention of Depression

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
Apr 20, 2010
Registry last updated
Mar 24, 2017

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.

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