MedPath

Connect ME: Improving Social Connectedness

Not Applicable
Completed
Conditions
Social Connectedness
Interventions
Behavioral: Brief Behavioral Activation for Improving Social Connectedness
Registration Number
NCT05686681
Lead Sponsor
Dartmouth-Hitchcock Medical Center
Brief Summary

To assess the reach and effectiveness of a behavioral activation intervention for older adults experiencing low social connectedness by Area Agency on Aging Staff.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
11
Inclusion Criteria
  • Older adults (age>60) will be enrolled because they are the target population served by the home-delivered meals program and the target sample for this study.
Exclusion Criteria
  • Clinically significant depression (Patient Health Questionnaire; PHQ-9 ≥ 10) or active suicide risk (Columbia Suicide Severity Rating Scale; C-SSRS), or Cognitive Impairment (Blessed Orientation-Memory-Concentration Test>9)
  • Clients who score 1 or greater on question 9 of the PHQ-9 will be further assessed for suicide risk using the Columbia-Suicide Severity Rating Scale (C-SSRS)
  • Clients will meet exclusion criteria for a positive response to any item
  • We will exclude older adults with uncorrectable hearing or vision impairment rendering them unable to use the tele-conferencing equipment.
  • Those who cannot speak English and have impaired decision-making capacity
  • Adults unable to consent will be excluded
  • Individuals who are not yet adults (infants, children, teenagers) will be excluded
  • Pregnant women will be excluded
  • Prisoners will be excluded

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Brief Behavioral Activation for Improving Social ConnectednessBrief Behavioral Activation for Improving Social ConnectednessActive, 6 session Brief Behavioral Activation for Improving Social Connectedness
Primary Outcome Measures
NameTimeMethod
Social Connectedness B, Baselinebefore the intervention

8-item PROMIS Social Isolation Scale

Social Connectedness A, Change from Post Intervention to Follow Up12 weeks post intervention

10-item Duke Social Support Index (DSSI)

Social Connectedness B, Change from Baseline to Post Interventionimmediately following the intervention

8-item PROMIS Social Isolation Scale

Social Connectedness A, Change from Baseline to Post Interventionimmediately following the intervention

10-item Duke Social Support Index (DSSI)

Social Connectedness A, Baselinebefore the intervention

10-item Duke Social Support Index (DSSI)

Social Connectedness B, Change from Post Intervention to Follow Up12 weeks post-intervention

8-item PROMIS Social Isolation Scale

Secondary Outcome Measures
NameTimeMethod
Intervention Reach12 Months

Reach will be determined by the proportion of eligible agency clients who agree participate in the study.

Trial Locations

Locations (1)

Dartmouth-Hitchcock Medical Center

🇺🇸

Lebanon, New Hampshire, United States

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