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NCT06746155Recruiting

Predictors of Relapse in Major Depressive Disorder (PERFORM-D)

Predictors of Early Relapse During Follow-up Of Remitted Major Depression

Source: ClinicalTrials.gov · Last updated 10 Jul 2026

Brief summary (registry, in English)

Major depressive disorder (MDD) is a common condition involving recurring periods of depression. One of the major challenges faced by people with MDD is that the episodes of depression tend to recur even after they are successfully treated. Currently, it is hard to predict when a depressive episode will recur. Being able to forecast this would help healthcare providers monitor patients and prevent relapse. The purpose of this study is to monitor features such as clinical symptoms, physical activity, sleep patterns, cognitive functioning and brain activity to help us understand how relapse happens and the mechanisms that cause it. From these different types of data, investigators will build a model that tells us who is more likely to experience a relapse and when the relapse is likely to occur. This study will be a significant step forward in understanding and managing MDD. Investigator will create a practical tool that will allow healthcare providers to monitor patients more effectively. By identifying early signs of relapse, investigators may be able to intervene promptly to prevent depressive episodes. Finally, our research will help understand the factors that underlie relapse in MDD, which will encourage the development of novel treatment approaches.

Status (registry)
Recruiting
Study type
Observational
Enrollment
252 (estimated)
First submitted
30 Oct 2024
Start date
27 Dec 2024
Primary completion date
1 Oct 2028
Lead sponsor
Abraham Nunes
Diseases
Depression
NCT number
NCT06746155

What you commit to

  • Study type: Observational
  • Planned participants: 252
  • From 27 Dec 2024 to the primary completion date, 1 Oct 2028
  • 9 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Bipolar I or Bipolar-II diagnosis (lifetime), schizophrenia, or schizoaffective disorder.
  • Existence of major neurological disorders, head injury (if accompanied by any of \[A\] loss of consciousness longer than 24 hours, \[B\] documented evidence of Glasgow Coma Scale \<9 at the time of injury, \[C\] post-traumatic amnesia lasting longer than 24 hours) (43), or other unstable medical conditions.
  • The participant presents with any condition which, according to the researcher's judgment, could interfere with the assessments stipulated in the protocol.

Other

  • Elevated risk of suicide, as determined by clinical evaluation.
  • The participant is employed by the researcher, actively involved in the current study or other research overseen by the same researcher, or is a relative of a study employee or the researcher.

Who the study is looking for

  • Outpatients 18 to 70 years of age.
  • Meet DSM-V criteria for MDD as determined by the SCID-5 or other standardized clinical interviews.
  • In the current or most recent MDE, participant must be responding or responded to a treatment or a combination of treatments for MDD. Patients with remitted MDD who are currently not taking medications will also be accepted. Patients must have achieved remission at or later than May 1, 2023.
  • Participants must have a MADRS total score ≤14.
  • Participant must be willing and able to complete self-reported assessments including sufficient fluency in English.
  • Participant must be willing to wear the wrist-worn actigraphic device for the duration of the study.

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Of Calgary
Coordinator of this site? Confirm its status
CalgaryCanadaRecruiting
Nova Scotia Health
Coordinator of this site? Confirm its status
HalifaxCanadaRecruiting
McMaster University
Coordinator of this site? Confirm its status
HamiltonCanadaRecruiting
Queen's University
Coordinator of this site? Confirm its status
KingstonCanadaRecruiting
The Royal Ottawa Mental Health Centre
Coordinator of this site? Confirm its status
OttawaCanadaNot yet recruiting
Centre for Addiction and Mental Health (CAMH)
Coordinator of this site? Confirm its status
TorontoCanadaRecruiting
University Health Network
Coordinator of this site? Confirm its status
TorontoCanadaRecruiting
University of British Columbia
Coordinator of this site? Confirm its status
VancouverCanadaRecruiting
Ontario Shores Centre for Mental Health Sciences
Coordinator of this site? Confirm its status
WhitbyCanadaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.