Intervention to Address Psychosocial Needs Among Socially Disadvantaged Older Adults With Cancer

Sponsor
UNC Lineberger Comprehensive Cancer Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05828654
Collaborator
(none)
25
1
1
6.6
3.8

Study Details

Study Description

Brief Summary

The purpose of this study is to convene a group of diverse North Carolina-based community representatives (patients, caregivers, leaders of faith-based organizations, social workers, and patient navigators) to inform the adaptation of materials used to train lay navigators in the delivery of psychosocial support interventions tailored to older socially disadvantaged adults with cancer.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Focus Group Discussions and Semi-structured Interviews
  • Behavioral: Training community lay navigators
N/A

Detailed Description

This behavioral study will explore community representatives' perspectives on the resources and training needed to support the development of a lay navigation program tailored to older socially disadvantaged adults with cancer.

It was hypothesized that diverse community representatives could inform the adaptation of training materials (Peer Connect) and subsequent training of community lay navigators, who will then be positioned to address the psychosocial needs of older adults with cancer

Study Design

Study Type:
Interventional
Anticipated Enrollment :
25 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Adapting Peer Connect to Train Lay Navigators in Delivering Psychosocial Support to Older Adults With Cancer
Anticipated Study Start Date :
Apr 15, 2023
Anticipated Primary Completion Date :
Nov 1, 2023
Anticipated Study Completion Date :
Nov 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: Single Arm

Community representatives

Behavioral: Focus Group Discussions and Semi-structured Interviews
Community representatives will be asked to participate in either 1:1 semi-structured interviews with a research staff member or to engage in focus group discussions with other community members. These interviews and discussions will gather broad perspectives on resource and training needs for community lay navigators and inform the adaptation of existing Peer Connect training materials

Behavioral: Training community lay navigators
Lay navigators identified from among the recruited community representatives will be trained either in-person or virtually by research staff members in motivational interviewing and other strategies to provide psychosocial support to older socially disadvantaged adults with cancer. For community lay navigators and inform the adaptation of existing Peer Connect training materials.

Outcome Measures

Primary Outcome Measures

  1. Adaptation of the existing Peer Connect training materials- interviews [12 months]

    Through semi-structured interviews, feedback will be qualitatively collected from community representatives to guide the adaptation and further refinement of lay navigator training materials.

  2. Adaptation of the existing Peer Connect training materials- focus group discussions [12 months]

    Through focus group discussions, feedback will be qualitatively collected from community representatives to guide the adaptation and further refinement of lay navigator training materials.

Secondary Outcome Measures

  1. Training community lay navigators- training sessions [12 months]

    The ability to train community lay navigators using the newly adapted training content- training sessions will be assessed by the number of training sessions completed by lay navigators and the research staff, allowing for sharing of broad perspectives on training methods, content, and delivery.

  2. Training community lay navigators - semi-structured interviews [12 months]

    The ability to train community lay navigators using the newly adapted training content will be assessed through qualitative semi-structured interviews with lay navigators and the research staff, allowing for sharing of broad perspectives on training methods, content, and delivery.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion criteria to participate in the study:
  1. Patients aged 65 and older diagnosed with hematological cancer for at least one year with stable disease

  2. Community representative 18 years or older who also identifies as at least one of the following:

  3. Cancer caregivers

  4. Social workers, social work students, or patient navigators Community leader (e.g., leader of a faith-based organization)

  5. Previously or currently serve as a lay navigator/peer supporter, community health worker, or coach

  6. Have personal experience with any of the following (being Black race, previously or currently facing socioeconomic challenges, or living in a rural community)

  7. Patient or community representative who is Able to understand and speak in English

Exclusion Criteria

All participants meeting any of the following exclusion criteria at enrollment will be excluded from the study:

  1. Inability to read and speak English

  2. Dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent

Exclusion Criteria

All participants meeting any of the following exclusion criteria at enrollment will be excluded from the study:

  1. Inability to read and speak English

  2. Dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Lineberger Comprehensive Cancer Center, UNC Chapel Hill North Carolina United States 27514

Sponsors and Collaborators

  • UNC Lineberger Comprehensive Cancer Center

Investigators

  • Principal Investigator: Shakira Grant, MD, UNC Lineberger Comprehensive Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
UNC Lineberger Comprehensive Cancer Center
ClinicalTrials.gov Identifier:
NCT05828654
Other Study ID Numbers:
  • LCCC2240
First Posted:
Apr 25, 2023
Last Update Posted:
Apr 25, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by UNC Lineberger Comprehensive Cancer Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 25, 2023