- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02302248
Effectiveness of a Crowdsourced Cognitive Reappraisal Intervention
A Randomized, Active-Controlled Trial to Investigate the Effectiveness of a Crowdsourced Cognitive Reappraisal Intervention.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
There are many ways to manage stress and mood, including exercise, diet, and relaxation practices. Cognitive-based techniques are also extremely powerful. Simply changing how you think about stressful situations can dramatically affect the way you feel. Individuals who routinely use strategies like cognitive reappraisal exhibit an enviable affective profile: studies suggest these individuals generally have less stress, lower incidence of depression, and better social functioning than those who rely on less adaptive emotion regulatory techniques. Techniques like cognitive reappraisal are also integral to many evidence-based psychotherapeutic traditions, such as cognitive-behavioral therapy and rational-emotive therapy.
Unfortunately, cognitive techniques can be hard to learn. Thinking flexibly about stressful thoughts and situations requires creativity and poise, faculties that often elude us when we need them the most. In this study, the investigators evaluate a web-based technology that uses crowdsourcing and peer-to-peer interactions to help people learn cognitive-based techniques and apply them throughout their daily lives.
The goal of the proposed study is to see whether the investigators' technology is more engaging and more effective at reducing depression symptoms than a web-based expressive writing platform. While the investigators are most interested in how this intervention affects depression symptoms, the investigators will also assess other psychological variables and the investigators will open the study to the general population.
Participation in this study will last three weeks. Participants will be randomly assigned to receive either a crowdsourcing reappraisal platform or an expressive writing platform. All study procedures (subject recruitment, baseline and follow-up assessments, interventions) will be conducted online.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- An email account, a desktop computer, and broadband Internet access
- Access to modern web browsers (e.g., Chrome, Safari, Firefox)
- Native English speaker
- 18 to 35 years old
Exclusion Criteria:
- Planning to be without Internet access during the scheduled intervention time
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Crowdsourced Reappraisal
Participants received the web-based crowdsourcing reappraisal intervention.
|
3 week access to a web-based crowdsourcing reappraisal platform.
|
Active Comparator: Expressive Writing
Participants received the web-based expressive writing intervention.
|
3 week access to a web-based expressive writing platform.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Center for Epidemiologic Studies Depression Scale
Time Frame: Baseline and 3 weeks
|
Baseline and 3 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Emotion Regulation Questionnaire
Time Frame: Baseline and 3 weeks
|
Baseline and 3 weeks
|
|
Perseverative Thinking Questionnaire
Time Frame: Baseline and 3 weeks
|
Baseline and 3 weeks
|
|
Subjective Happiness Scale
Time Frame: Baseline and 3 weeks
|
Baseline and 3 weeks
|
|
Positive and Negative Affect Schedule
Time Frame: Baseline and 3 weeks
|
Baseline and 3 weeks
|
|
Utilization and Attrition
Time Frame: Baseline-week 3
|
activity level (word count, number of social actions, average number and length of web sessions)
|
Baseline-week 3
|
Collaborators and Investigators
Investigators
- Principal Investigator: Rosalind W Picard, Sc.D, Massachusetts Institute of Technology
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1311006002
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Depression
-
ProgenaBiomeRecruitingDepression | Depression, Postpartum | Depression, Anxiety | Depression Moderate | Depression Severe | Clinical Depression | Depression in Remission | Depression, Endogenous | Depression ChronicUnited States
-
Washington University School of MedicineCompletedTreatment Resistant Depression | Late Life Depression | Geriatric Depression | Refractory Depression | Therapy-Resistant DepressionUnited States, Canada
-
Kintsugi Mindful Wellness, Inc.Sonar Strategies; Vituity PsychiatryRecruitingDepression | Depression Moderate | Depression Severe | Depression MildUnited States
-
University of California, San FranciscoRecruitingDepression Moderate | Depression Mild | Depression, TeenUnited States
-
University GhentUniversiteit Antwerpen; Janssen-Cilag Ltd.RecruitingDepression Moderate | Depression Severe | Depression MildBelgium
-
Baylor College of MedicineUniversity of TexasRecruitingDepression | Depression Moderate | Depression Severe | Suicide and Self-harm | Depression in Adolescence | Depression MildUnited States
-
University of Cape TownNational Institute of Mental Health (NIMH)CompletedPostpartum Depression | Clinical Depression | Moderate DepressionSouth Africa
-
Lawson Health Research InstituteTerminated
-
Washington University School of MedicinePatient-Centered Outcomes Research Institute; National Institute of Mental...CompletedMajor Depressive Disorder | Treatment Resistant Depression | Treatment-Refractory Depression | Late Life Depression | Geriatric DepressionUnited States, Canada
-
Northern Illinois UniversityUniversity Autonoma de Santo DomingoTerminatedDepression Moderate | Depression MildUnited States, Dominican Republic
Clinical Trials on Crowdsourcing reappraisal intervention
-
University Hospital Southampton NHS Foundation...Completed
-
Shenzhen Kangning HospitalScience and Technology Innovation Commission of Shenzhen MunicipalityNot yet recruiting
-
Weill Medical College of Cornell UniversityNational Institute of Mental Health (NIMH); Stanford University; Florida State... and other collaboratorsRecruitingSuicide PreventionUnited States
-
University of DenverWake Forest UniversityRecruiting
-
Wake Forest University Health SciencesWake Forest UniversityWithdrawn
-
Medical University of GrazUniversity of GrazRecruitingFunctional Movement DisorderAustria
-
Ekaterina PogrebtsovaCompletedMental Health Wellness 1
-
Icahn School of Medicine at Mount SinaiCompletedBorderline Personality Disorders | Avoidant Personality DisordersUnited States
-
University of BernUniversity of Vienna; Center for Primary Care and Public Health (Unisante),...CompletedStress ReactionSwitzerland