Local research. Human connections. WCR Miami Lakes (786) 483-7856
Back to study searchNCT06358404
Active, not recruitingNCT06358404ClinicalTrials.gov record

Developing a Peer Support Intervention for Depression in SCD

Subjective Cognitive Decline · Depression in Old Age

THE QUICK READ

What this study involves

The registry does not currently label this study as recruiting. Ask about its status before planning a screening visit.

Study type
Interventional
Phase
Not applicable
Age range
60 years - Not specified
Sex eligible
All sexes
Healthy volunteers
Not accepted
Participants
30 Estimated

These are starting points, not an eligibility decision. The research team must review the full requirements.

About the research

The purpose of this study is to assess the feasibility, acceptability, and fidelity of an 8-week intervention where peer coaches will deliver depression care to adults 60 years of age or older who have depression and subjective cognitive decline.

Read the full description

With support from the MADRC ORE Core, we will recruit 30 community-dwelling older adults to conduct an open pilot study of PeersCOG. Trained and supervised peer coaches will deliver depression care to adults 60 years of age and older with depression and subjective cognitive decline in an 8-week intervention using video chats and texts. We will use mixed methods to assess feasibility, acceptability, and fidelity. We will use validated instruments to assess the preliminary outcomes, including depression, SCD, functioning, and social factors at baseline, 8 weeks, and 3 months, and we will conduct post-intervention interviews with stakeholders at 8 weeks. Older adult participants will be asked to name a study partner who will support the older adult throughout the study in terms of study enrollment. They may also have additional perspectives on the impact of impaired cognition and depression on daily living and related needs. The older adult will not be excluded if the study partner is not available.

Who may be able to participate?

The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.

Inclusion Criteria:

  • Older adults aged 60+
  • Endorse subjective cognitive decline
  • Endorse depressive symptoms
  • not currently experiencing suicidal ideation nor active, untreated manic, psychotic, or substance use disorder
  • fluent in English and able to give informed consent

Exclusion Criteria:

  • Meets diagnostic criteria for mild cognitive impairment or Alzheimer's dementia
  • Meets diagnostic criteria for a current major depressive disorder
  • have a history of neurological and psychiatric comorbidities such as major depressive disorder in the past 12 months
Understand screening

Treatment, groups and participation

The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.

Assignment
Not applicable
Masking
No masking
Intervention

Peer coaches will deliver the PeersCOG intervention to participants.

Behavioral: PeersCOG

PeersCOG BEHAVIORAL

. The intervention will consist of 8 weekly video chats focused on emotional, appraisal, and informational support delivered by community-based older adult peer coaches to adults 60 years of age and older with subthreshold depression and SCD.

Prepare your questions

What researchers are measuring

Outcome measures describe what is being studied. They are not proof that a treatment works.

Primary measures

Feasibility of Intervention

Time frame: Measured at baseline enrollment

Level of participant engagement: how many screened older adults agree to participate in the intervention and complete baseline assessments

Acceptability of Intervention

Time frame: Measured during intervention (8 weeks)

Number of meetings older adults complete with peer coach

Fidelity of Intervention

Time frame: Measured during intervention (8 weeks)

Degree of adherence to intervention

No results are flagged as posted.

Review the complete result tables and limitations in the official record.

Open official results ↗

Research locations (1)

The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.

1 locations

Massachusetts General HospitalBoston, Massachusetts, United StatesStatus unknown

Study team and timeline

Lead sponsor
Massachusetts General Hospital
Study start
May 1, 2024 Actual
Primary completion
May 31, 2027 Estimated
Study completion
May 31, 2027 Estimated
First posted
Apr 10, 2024 Actual
Last updated
Nov 9, 2026 Actual

Official study contacts

No central contact is listed. Check the locations and the official record.

Official study title

Developing a Peer Support Intervention for Depression in SCD

A HUMAN NEXT STEP

Ask Wellness Clinical Research

Your message goes to WCR, including when this study is run by another organization. WCR may offer general guidance but may not operate this trial, have access to its team or be able to enroll you.

Please do not include medical records, diagnoses, medications, insurance numbers or other sensitive details. This form is for general questions, not urgent care.

Sending a question does not enroll you in a trial.

Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.

Retrieved: Nov 12, 2026 · Last registry update: Nov 9, 2026