Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
All Genders
NCT06510439

Need to be Needed (N2BN) Intervention

Led by Temple University · Updated on 2026-01-21

120

Participants Needed

1

Research Sites

555 weeks

Total Duration

On this page

Sponsors

T

Temple University

Lead Sponsor

N

National Institute on Disability, Independent Living, and Rehabilitation Research

Collaborating Sponsor

AI-Summary

What this Trial Is About

The proposed study is a randomized, controlled trial (RCT) that will examine the effectiveness of an intervention designed to reduce social isolation and loneliness of adults with serious mental illness (SMI). The intervention will focus on improving their sense of mattering by using acts of kindness and experiencing gratitude through volunteering. 120 participants will be randomly assigned to the intervention group or the attention control group. Over the course of the 6-month intervention, participants in the intervention arm, will receive weekly support from the interventionist. The interventionist and the participant will collaboratively set goals and develop an initial intervention plan, which is informed by the participants interests, values and goals. The attention control group will receive non-directive listening support through research assistants. Data collection for all participants will occur at baseline, at the mid-point of the intervention at 3 months, and at the end of the 6-month intervention. Participants will be asked questions about quality of experience, social context and satisfaction, mattering components, kindness, gratitude, and loneliness. We will gather data on demographic background, life transitions, social network characteristics, internalized stigma, neighborhood climate, depression, and trait measures of mattering and loneliness during intake and exit interviews. Additionally, participants of the intervention arm will be asked to provide feedback about the intervention.

CONDITIONS

Official Title

Need to be Needed (N2BN) Intervention

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with Major Depression, Bipolar I, Bipolar II, or Schizophrenia Spectrum disorder by research staff
  • Aged 18 years or older
  • Living in the community
  • Able to communicate in written and oral English
  • UCLA-Loneliness Scale score of 6 or higher
Not Eligible

You will not qualify if you...

  • Having a legal guardian
  • Unable to give informed consent
  • Living situation restricts ability to move freely
  • Enrollment of vulnerable populations is not allowed

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hall Mercer

Philadelphia, Pennsylvania, United States, 19106

Actively Recruiting

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Research Team

B

Bryan Mccormick, PhD

CONTACT

T

Tabea Neumann, M.Sc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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