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Self-reported Symptoms of DepressionNCT06631183

Behavioral Study to Predict the Efficacy of a Self-Help Tool

A study testing Self-help information based on principles of behavioral activation and Self-help information based on principles of cognitive restructuring in people with Self-reported Symptoms of Depression, run by Trustees of Princeton University at 1 site in United States.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

The study aims to examine whether the investigators can predict, on the level of individual participants who have symptoms of depression, who will benefit more from self-help tools based on principles of behavioral activation vs. cognitive restructuring, in terms of a greater decrease of self-reported symptoms. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Self-reported Symptoms of Depression
What is being tested?
Self-help information based on principles of behavioral activation and Self-help information based on principles of cognitive restructuring
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,500 participants
Where
1 siteUnited States
Study dates
23 Jan 2024to Dec 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Fluent in English
  • The primary mental health concern participants want to work on must be that they would like to improve their mood, to reduce negative thoughts, to enjoy more activities again and/or to reduce symptoms of depression
  • Having a picture ID and be willing to meet with us on a video zoom call for identity verification if invited to do so

Who cannot join

  • Lack of attention when completing parts of the study, lack of honesty or not completing parts of the study in a timely way
  • Identity check failure

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Princeton Neuroscience Institute, but recruitment and study are conducted completely online and can occur anywhere in the US.

    Princeton, New Jersey, 08540

Other trials in United States

About this study

The study aims to examine whether the investigators can predict, on the level of individual participants who have symptoms of depression, who will benefit more from self-help tools based on principles of behavioral activation vs. cognitive restructuring, in terms of a greater decrease of self-reported symptoms. The investigators use a combination of self-reported clinical information and behavior on learning and decision-making tasks to predict change in symptom scores.

Read the detailed description

Background:

Cognitive-Behavioral Therapy (CBT) is a learning-based psychotherapy treatment that has been established as effective treatment for depression. It consists of two core interventions: cognitive restructuring (CR) and behavioral activation (BA). In recent years, internet-delivered CBT (iCBT) has been developed, which allows for dissemination of standardized, evidence-based, CBT treatments at scale.

Virtually all psychotherapy methods aim to teach clients something new: new behavioral or thought patterns, new responses to triggers and situations, and/or new emotional reactions. As such, learning-based psychotherapies modify targeted brain circuits to the extent that these circuits show flexibility and are amenable to change through learning. The human brain has several learning circuits/mechanisms that work in parallel. Different people will have more flexibility and learn more effectively through some learning mechanisms and not others. Because different psychotherapy methods (e.g., BA and CR) rely on different types of learning, the investigators hypothesize that by characterizing what learning mechanisms are most available and efficient for each person, will allow us to predict what intervention method will be most effective for that person.

The goal of this study is to test if people's individual learning propensities can predict what type of intervention will benefit them more.

Detailed study design:

In a fully online study, the investigators deploy several behavioral tasks to assess individual differences in learning and decision-making processes. Participants then get access to an internet-based self-help tool for depression that is based on CBT principles, and are asked to undergo either the BA modules or the CR modules (random assignment; 5 weeks of 1-hour session per week). The investigators follow up on symptoms at the middle of the period of use of the self-help tool (at this point, some behavioral tasks are repeated as well), at the end of this period, and at different times up to a year after finishing use of the self-help tool.

Participants are recruited online via advertisement, for instance on social media. After checking eligibility and obtaining consent online, participants are randomized to be part of the discovery or validation dataset (the investigators will not analyze the validation dataset until all analyses are pre-registered). Participants are then asked to fill out a range of symptom self-report questionnaires and complete a series of behavioral tasks. They are then randomized to either a cognitive restructuring group or behavioral activation group. All participants are then given access to e-couch, a validated self-help tool. In the first week, all participants complete the depression information submodule from the depression program. Over the following four weeks, participants in the cognitive restructuring group complete submodules on cognitive restructuring and participants in the behavioral activation group complete submodules on behavioral activation and physical activity. After that period, participants are free to engage with any of the other modules e-couch offers. Participants are additionally asked to fill out symptom self-report questionnaires 1,3,5,12,24 and 48 weeks after the start of e-couch engagement, and to repeat a subset of the behavioral tasks 3 weeks after the start of e-couch engagement.

All interaction with participants is conducted online via email (and possibly via zoom to verify identity or technical advice) and online-administered tasks, questionnaires and the self-help tool. The investigators do not offer any medical advice and forward participants to appropriate sources of support (e.g., hotlines) if needed.

Quality assurance plan:

All data are collected online through our in-house custom-built software. The code for the assessments has been reviewed and data quality has been checked prior to study start. The code is backed up on a secure server and the investigators can make the code available for review to relevant authorities.

Data checks:

The investigators use a range of attention checks throughout the study to exclude data from inattentive participants or participants who respond randomly.

Statistical analysis plan:

Note, the goal of this study is not to assess how much the self-help tools affect symptoms on average. This has been examined previously (and will only be verified in this dataset). The primary goal of this study is to develop a tool that predicts for a new individual (whose data was not part of the tool development, i.e. out-of-sample) what interventions they may benefit more from.

When consenting, participants are assigned to a discovery or a validation dataset. After completing analyses on the discovery dataset, the investigators will pre-register a detailed statistical analysis plan and apply that to the validation dataset to confirm and verify any findings. Below is the general approach to analyzing the discovery data:

Step 1) Compute scores for the self-report scales in line with the literature and fit computational models to data from the behavioral task to retrieve individual model parameters that best explain behavior the behavior from each participant.

Step 2) Use prediction models, e.g. elastic nets, to predict from the above parameters and scores, symptom scores (in particular, for depression and anhedonia) from each participant at the end of the engagement with the self-help tool and during follow ups, and/or improvement of symptom scores from before to after the engagement with the self-help tool.

Step 3) Examine whether change in task behavior due to the first half of engagement with the self-help tool mediates a change in symptoms from before to after that engagement.

Being tested
Self-help information based on principles of behavioral activation, Self-help information based on principles of cognitive restructuring

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Self-help information based on principles of behavioral activationBehavioural

    Participants will engage with the self-help tool e-couch (https://ecouch.com.au). In the first week, they will complete the depression information submodule from the depression program. Over the following four weeks, they will complete submodules on behavioral activation and physical activity.

  • Self-help information based on principles of cognitive restructuringBehavioural

    Participants will engage with the self-help tool e-couch (https://ecouch.com.au). In the first week, they will complete the depression information submodule from the depression program. Over the following four weeks, they will complete submodules on cognitive restructuring.

Study groups in NCT06631183
Study groupRoleWhat they receive
Behavioral activation groupExperimentalParticipants will read information and engage in exercises through the self-help tool e-couch that aim at stimulating their engagement in pleasant activities.
Receives: Behavioral: Self-help information based on principles of behavioral activation
Cognitive restructuring groupExperimentalParticipants will read information and engage in exercises through the self-help tool e-couch that aim at tackling negative thinking.
Receives: Behavioral: Self-help information based on principles of cognitive restructuring

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Predictive accuracy of sum of self-reported depression symptoms (assessed with Patient Health Questionnaire) after engagement with self-help tool using behavioral tasks

    Participants will be randomized to a discovery or validation datasets with a ratio of 2:1. Prior to analyzing the validation dataset, the investigators will pre-register the precise analyses based on the results from the discovery dataset. Participants complete several behavioral tasks focusing on learning and decision-making prior to start of the engagement with the self-help tool. Self-reported depression symptom scores are assessed with the Patient Health Questionnaire (PHQ-9, sum ranges from 0-27, higher scores indicate more symptoms of depression). The investigators will predict change in depression symptoms based on modeled task data and then verify the results in pre-registered analyses of the validation dataset.

    Measured: approx. 6 weeks

  2. Predictive accuracy of sum of self-reported anhedonia symptoms (assessed with Snaith-Hamilton Pleasure scale) after engagement with self-help tool using behavioral tasks

    Participants will be randomized to a discovery or validation datasets with a ratio of 2:1. Prior to analyzing the validation dataset, the investigators will pre-register the precise analyses based on the results from the discovery dataset. The participants complete several behavioral tasks focusing on learning and decision-making prior to start of the engagement with the self-help tool. Self-reported symptoms scores of anhedonia will be assessed with the Snaith-Hamilton Pleasure Scale (SHAPS, sum score range from 14-56, higher scores indicate more anhedonia). The investigators will predict change in anhedonia symptoms based on task data and then verify the results in pre-registered analyses of the validation dataset.

    Measured: approx. 6 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Oct 2024
  2. Study start23 Jan 2024
  3. Primary completionDec 2025 (estimated)
  4. Study completionDec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Care provider, Outcomes assessor
Enrolment
1,500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06631183
Sponsor's protocol ID
15118
Status last verified
Apr 2025
First submitted
24 Sep 2024
Last updated
10 Apr 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Researchers will share de-identified questionnaire data and behavioral task data with other researchers from the Wellcome Leap consortium and after publication with other researcher upon reasonable request.

Publications

  • Ding J, Chiu JC, Moon S, Ren Y, Turner DM, Shoval G, Niv Y, Berwian IM. Protocol for a randomized trial to predict the efficacy of cognitive and behavioral interventions for symptoms of depression. Front Psychiatry. 2026 Apr 16;17:1774560. doi: 10.3389/fpsyt.2026.1774560. eCollection 2026.

    PubMed 42079320

Questions about this trial

What is this clinical trial studying?

A study testing Self-help information based on principles of behavioral activation and Self-help information based on principles of cognitive restructuring in people with Self-reported Symptoms of Depression, run by Trustees of Princeton University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 10 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Predictive accuracy of sum of self-reported depression symptoms (assessed with Patient Health Questionnaire) after engagement with self-help tool using behavioral tasks (time frame: approx. 6 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06631183, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Apr 2025.

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