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Social Connections and Healthy Aging (The Senior Connection)

Social Connections and Healthy Aging (The Senior Connection)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01408654
Acronym
TSC
Enrollment
368
Registered
2011-08-03
Start date
2011-09-30
Completion date
2016-03-31
Last updated
2016-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Suicidal Ideation

Keywords

Suicidal Ideation, Loneliness, Social Support, Voluntary Workers, Friends/Companions, Prevention, Aged

Brief summary

This randomized trial compares peer companionship to care-as-usual in primary care on the outcome of risk for suicidal behavior in late life. The investigators hypothesize that older adults assigned to receive peer companionship will report greater social connectedness and less death and suicidal ideation compared to older adults assigned to care as usual.

Detailed description

There is a pressing need for interventions that reduce risk for suicide in later life. Older adults in the U.S. have the highest rate of suicide and are the fastest growing segment of the population. The investigators can anticipate a large rise in the number of older adults who die by suicide in coming decades. This application is in response to RFA-CE-10-006. Consistent with the CDC's key strategy of reducing suicide by promoting connectedness, our long-term goal is to reduce late life suicide-related morbidity and mortality by leveraging the resources and expertise of the aging services provider network (ASPN) to address unmet social needs of community-dwelling older adults. Our objectives with this proposal are (1) to examine whether linking socially disconnected seniors with peer supports through the Retired and Senior Volunteer Program (RSVP) is effective in reducing risk for suicide, and (2) to test an hypothesized mechanism for the association of social disconnectedness and suicidal ideation and behavior informed by the Interpersonal Theory of Suicide. The investigators will recruit 400 primary care patients (200 men and 200 women) over age 60 years who endorse feeling lonely and/or as if they are a burden on others. They will be randomly assigned to either of two conditions. Those assigned to The Senior Connection (TSC) will either be paired with a peer companion or, if they prefer and are eligible, be trained and placed as a peer companion for others by RSVP. The comparison group will receive no further intervention (care-as-usual \[CAU\]). Subjects will be followed for up to 24 months with repeated in-home (baseline, 12, and 24 months) and telephone assessments (3, 6, and 18 months).

Interventions

BEHAVIORALPeer Companionship

Peer companionship is provided at least four times per month over two years in the form of friendly visiting, supportive phone calls, and some instrumental support.

Sponsors

Centers for Disease Control and Prevention
CollaboratorFED
University of Rochester
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 60 or older * Primary Care Patient * Endorses feeling lonely and/or like a burden in the the past two weeks

Exclusion criteria

* Positive dementia screen * Current alcohol abuse * Psychosis * Suicidal ideation with intent to act (current or past month.)

Design outcomes

Primary

MeasureTime frameDescription
Suicidal IdeationBaseline, 3,6,12,18,24 monthsSeverity of suicidal and death ideation assessed with the Geriatric Suicide Ideation Scale

Secondary

MeasureTime frameDescription
Social ConnectednessBaseline, 3,6,12,18,24 monthsThwarted belongingness and perceived burdensomeness assessed by the Interpersonal Needs Questionnaire.
ConnectednessBaseline, 3,6,12,18,24 monthsSocial network size/density/quality assessed with the National Social Life, Health, and Aging Project Social Network Module.
DepressionBaseline, 3,6,12,18,24 monthsAssessed with the PHQ-9

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026