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A Pilot Randomized Controlled Trial of the Hopeful and Healthy Living Program

Enhancing Social Connection, Health, and Aging in Older Persons: A Pilot Randomized Trial of the Hopeful and Healthy Living (HHL) Program

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06940843
Acronym
(HHL)
Enrollment
60
Registered
2025-04-23
Start date
2025-03-12
Completion date
2028-07-31
Last updated
2026-07-20

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

Conditions

Older Adults, Serious Mental Illness

Keywords

psychosocial interventions, cognitive interventions, social skills interventions, healthy lifestyle interventions, older adults with SMI

Brief summary

The goal of this clinical trial is to learn if a novel psychosocial intervention is effective in helping adults over 50 with serious mental illness (SMI) increase their social connections and participate in more healthy lifestyle activities. The Hopeful and Healthy Living (HHL) intervention combines social skills training and training in cognitive self-management strategies in order to help older adults build healthy lifestyle and social routines. We predict that: * Individuals who participate in the HHL intervention will improve more in perceived social support (i.e., what people get from relationships such as reliance, reassurance of worth, attachment) and loneliness at the 4-, 8-, and 12-month follow-up assessments than those who receive treatment as usual (TAU). * Individuals who participate in the HHL intervention will improve more in overall psychosocial functioning at the 4-, 8-, and 12-month follow-up assessments than those who receive TAU. * Individuals who participate in the HHL intervention will improve more in cognitive functioning at the 4-, 8-, and 12-month follow-up assessments than those who receive TAU. * Individuals who participate in the HHL intervention will improve more in healthy behaviors (sleep, activity, diet) at the 4-, 8-, and 12-month follow-up assessments than those who receive TAU. In this trial, participants will be either receive the HHL intervention or participate in their regular treatment activities (treatment as usual). HHL vs. TAU will be compared to see if there are any differences in social support, cognition, loneliness, psychosocial functioning, or healthy lifestyle activities including physical activity, sleep, and diet. Participants will be asked to complete an interview-based assessment at baseline, 4-months, 8-months, and 12-months. After completing the baseline assessment, those who are in the experimental group will participate in the 16-week long HHL group intervention.

Interventions

BEHAVIORALHopeful and Healthy Living (HHL)

The HHL intervention is a 16-week long, manualized group intervention. Classes will be held weekly for 90 minutes. The class covers 15 topics centered on building social connections, developing healthy lifestyle routines around eating, exercise, and sleep. Each class will target one social skill (i.e. starting conversations) and one cognitive self-management strategy (i.e. memory tips), which will be taught and practiced in class. Each class also includes a facilitated exercise component and individually tailored take home application activity.

Sponsors

Boston University Charles River Campus
Lead SponsorOTHER
Bay Cove Human Services
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

50 years or older, diagnosis of a serious mental illness, and a member of Center Club or Transitions of Boston

Exclusion criteria

Diagnosis of dementia or other progressive neurological disorder

Design outcomes

Primary

MeasureTime frameDescription
Montreal Cognitive Assessment (MOCA)Baseline, 4-, 8-, 12- month followupStandardized screening tool used for assessing cognition.
The Cognitive Self-Efficacy ScaleBaseline, 4-, 8-, 12- month followup10-item measure that assesses confidence in everyday cognitive tasks.
The DSM-5-TR Self-Rated Level 1 Cross-Cutting Symptom MeasureBaseline, 4-, 8-, 12- month followupAdult will be used to assess and statistically control for mental health symptom severity.
The UCLA Loneliness Scale-3-item instrumentBaseline, 4-, 8-, 12- month followup3-item screening tool for loneliness.
The Social Provisions ScaleBaseline, 4-, 8-, 12- month followup24-item instrument that will be used to measure various types of social supports.
The Physical Activity Scale for the Elderly (PASE)Baseline, 4-, 8-, 12- month followupStandardized measurement of physical activity related to exercise, work, recreation, and daily living activities.
Starting the ConversationBaseline, 4-, 8-, 12- month followupA brief standardized survey for assessing daily eating habits.
Pittsburg Sleep Quality Index (PSQI)Baseline, 4-, 8-, 12- month followupAn 11-item tool that is used to assess sleep quality and routines.

Secondary

MeasureTime frameDescription
HHL Group Satisfaction and Feedback Survey4-month assessment onlyFor experimental group participants only.

Countries

United States

Contacts

CONTACTAlexa R Trolley-Hanson, MS OTR/L
athanson@bu.edu16037480379
CONTACTSusan McGurk, PhD
mcgurk@bu.edu617-353-3549
PRINCIPAL_INVESTIGATORSusan McGurk, PhD

Boston University

PRINCIPAL_INVESTIGATORKim Mueser, PhD

Boston University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 21, 2026