A New Model to Reach Vulnerable Older Adults With Pain Self-management Support

Chronic Pain Clinical Trial

Official title:

A New Model to Reach Vulnerable Older Adults With Pain Self-management Support

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04095650
• Other study ID #: HUM00154949
• Secondary ID: K01AG050706
• Status: Completed
• Phase: N/A
• Start date: September 20, 2019
• Est. completion date: May 14, 2020

Study information

• Verified date: January 2021
• Source: University of Michigan
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Learning chronic pain self-management skills can help patients improve daily functioning and quality of life, while avoiding risks associated with opioids and other pharmacological treatments. Community health workers (CHWs) may help make chronic pain self-management interventions more accessible to older adults living in underserved communities. The goal of this study is to conduct a feasibility test of a chronic pain self-management intervention delivered by CHWs, in conjunction with mobile health tools, in a sample of 25 older adults recruited from community sites in Detroit, Michigan. This study will involve the use of mixed quantitative and qualitative methods to assess participant engagement and satisfaction, and change in pain-related outcomes.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 38
• Est. completion date: May 14, 2020
• Est. primary completion date: May 14, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 60 Years and older

Eligibility

Inclusion Criteria:

• English-proficient

• Age >= 60 years

• Ambulatory with or without assistive device

• Community-living

• Have a cell or landline phone

• Have Internet access (home or elsewhere)

• Self-reported chronic musculoskeletal pain (pain in muscles or joints for > 3 months); >4 (0-10 scale) average pain level over last week; >1 day/previous 30 when pain made it difficult to do usual activities

• Ability to attend a one-time study orientation session

Exclusion Criteria:

• Serious acute illness or hospitalization in last month

• Planned surgery in next three months

• Significant cognitive impairment as indicated by affirmative response to question: "Do you have significant difficulties with your memory that get in the way of your usual daily activities?"

• Other severe physical or psychiatric disorder judged by study team to pose significant barrier to deriving program benefit.

Related Conditions & MeSH terms

• Chronic Pain

Intervention

Behavioral:
• STEPS (Seniors using Technology to Engage in Pain Self-management)
Participants will meet with a community health worker (CHW) at a one-hour in-person study orientation session. At this session, they will be introduced to the program, learn how to use the online modules and associated materials, and schedule six weekly telephone sessions with the CHW. Participants will be given a wearable physical activity tracker to use throughout the course of the program. They can choose to report daily step counts by automatically syncing to an app or via text message. Each week during the study period, participants will engage with content on the website, have a session with the community health worker, track their daily steps, and set and work toward pain-management goals.

Locations

Country	Name	City	State
United States	University of Michigan	Ann Arbor	Michigan

Sponsors (3)

Lead Sponsor	Collaborator
University of Michigan	American Pain Society, National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in pain interference	The Pain Interference 6-item subscale of the Patient-Reported Outcomes Measurement Information System (PROMIS)-43 Adult Profile. Items ask how much pain in the last 7 days has interfered with daily activities such as household chores and social activities (1=not at all to 5=very much); raw total scale scores range from 6 (low interference) to 30 (high interference)..	baseline and 8 weeks
Primary	Participant engagement	Number of completed sessions with the community health worker (range 1 to 7).	8 weeks
Secondary	Participant Global Impression of Change	Two items: 1) How participant thinks their pain has changed from baseline (much worse (-3) to much better(+3)). 2) How participant thinks their functioning has changed from baseline (much worse (-3) to much better(+3)).	8 weeks
Secondary	Participant satisfaction: Likert-scale questions	Likert-scale questions about participant satisfaction with the program; e.g., whether participation increased understanding of pain management (Strongly Agree=1 to Strongly Disagree=5), and with selected program elements (e.g., community health workers, videos, website).	8 weeks