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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06153199
Other study ID # IRB202300756
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 6, 2024
Est. completion date June 30, 2028

Study information

Verified date June 2024
Source University of Florida
Contact Kim Dunleavy, PT, PhD
Phone 13522736114
Email kdunleavy@phhp.ufl.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary purpose of this hybrid comparative effectiveness and implementation study is to compare two self-management strategies to manage pain, and adjust work-related ergonomic risk in nursery and landscape workers. This cluster randomized pragmatic study will compare interventions with different degrees of support and Specific aim 1 is to determine if self-management plus individualized guided participatory ergonomic choices (SM+PE) is more effective than self-management (SM) alone for improving LBP among horticulture workers. Both groups will review short self-management video modules to introduce general pain concepts and the importance of managing pain without medication, risks of opioid use, self-management of pain, and simple ergonomic strategies for both groups. Both groups will choose 1 self-management strategy to manage pain at home and 1 ergonomic workplace strategy to limit pain. The SM+PE participant's choices will be guided by researchers to match to their self-identified most difficult work activities due to pain and to those strategies that could be used more often rather than just their preferences. This group will also: 1) review videos of their work tasks, and 2) receive text reminders to support implementation. Surveys will include instruments reflecting low back pain disability, pain, work ability, and affective or cognitive characteristics (self-efficacy, pain anxiety, depression, coping), collected at baseline, pre- and post-intervention, with follow-ups at 3- and 6-months. Workers will be videoed pre- and post-intervention to inform simulated work analysis for calculation of work risk and to compare any changes for the most difficult tasks. Specific aim 2 will identify contextual factors impacting engagement, adoption, effectiveness, and implementation. Interviews, focus groups, and field notes will be used to explain results and establish patterns to inform future translation.


Description:

Primary dependent variables will be collected at all measurement points: pain severity, interference, and persistence, pain with specific work tasks, disability, work ability, and pain medication use. Affective or cognitive characteristics potentially impacting adoption and effectiveness (secondary dependent variables or confounders) such as coping, fear, anxiety, depression, will also be collected.The post- and follow-up survey questions will also reflect adoption, opinions of interventions, effectiveness, facilitators, and barriers.


Recruitment information / eligibility

Status Recruiting
Enrollment 164
Est. completion date June 30, 2028
Est. primary completion date June 30, 2028
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: Workers 1. working full time (30 hours or more per week) in physically demanding nursery or landscape work 2. currently employed or self-employed in small or medium size businesses 3. 18 years of age or older 4. English or Spanish speaking 5. experiencing continuous or intermittent LBP over the past 3 months Owners, managers, supervisors 1. Owners, managers, or supervisors who meet the same inclusion criteria as workers will be eligible to participate in the training interventions as well as the supervisory roles. 2. All owners, managers, and supervisors who are willing to participate will be enrolled. Exclusion Criteria: Workers 1. history of major trauma, surgery, or spinal nerve blocks in the past year 2. seeking disability or workman's compensation 3. self-disclosed pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Video training - Self-management
Short video modules on self-management of back pain without medication
Video training - Ergonomics
Short video module on ergonomic adjustment for limiting back pain in nursery and landscape work
Guided choice of ergonomic options matched to most difficult tasks
Guidance on ergonomic choices appropriate for work tasks not currently being used that are the most difficult due to back pain, using a checklist
Text reminders
Reminders to implement choices using graphics and gifs as well as motivational messages
Video review
Participants will review videos of their movement during their most difficult work tasks to help adjust ergonomic adjustments

Locations

Country Name City State
United States University of Florida Gainesville Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Florida

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Roland Morris Disability Index Disability Index for functional difficulties related to low back pain scored from 0-24 with low scores indicating lower disability 1 year
Primary Numeric Pain Rating Severity Severity of pain reported for the past week and for the 3 most difficult work activities 0=no pain, 100=worst imaginable pain, lower scores reflect lower pain 1 year
Primary Pain Interference Extent of pain interference with work activities in the past week, 0=not at all, 100=prevented working at normal level, lower scores reflect less interference 1 year
Primary Pain persistence Pain in the past 3 months reported on a 5 item scale ranging from not at all to pain every day without a break. 1 year
Primary Pain impact 2 items with 5 point scale recording impact on work activities and social activities ranging from never to always, with lower scores reflecting less impact 1 year
Primary Pain frequency Number of days in the past week pain is experienced ranging from 0-7 1 year
Primary Adoption Use of the interventions reported for each work or self-management strategy selected (number of days used in the past week, how often used (never, occassionally, consistently) Higher scores and consistently are optimal 1 year
Primary Difficulty with work tasks Patient Specific Functional Scale reported for 3 most difficult work activities with subscales reported on a scale of 0= no difficulty, 100=unable to perform with the average of the 3 items used for analysis. 1 year
Primary Work ability Work Ability short form is reported on numeric rating scale from 0 (completely unable to work) to 10 able to work at your best 1 year
Secondary Use of medication and substances Frequency of pain medication and substances for pain in past 3 months reported on a 4 item scale (never, 1-2 days, 3-4 days, 5-7 days) never is optimal. Items for alcohol, cannabis, tobacco, herbal products, acetaminophen, anti-inflammatories, muscle relaxants, opioids). Frequency of use per day on average also reported for a total estimate. 1 year
Secondary Depression scale Center for Epidemiology Depression Scale -Revised consists of 20 items reflecting frequency of depressive symptoms from rarely to most of the time with the total reported out of 60 with lower values as optimal 1 year
Secondary Pain anxiety Symptom Scale 20 item instrument with the total of items reported from never to always reported out of 50. Lower values are optimal. 1 year
Secondary Self-efficacy PROMIS short form 8a Self-efficacy chronic disease management 1 year
Secondary Self-efficacy and coping - confidence and control over pain Coping Skills Questionnaire reporting confidence to be able to work and live a normal lifestyle rated on a 6 point scale from 0=not at all confident to 5=completely confident (total reported out of 10, and 7 point scale for control over pain 0=no control, 6=completely in control. The total is reported out of 12 with higher values as optimal 1 year
Secondary Ergonomic risk Rapid Ergonomic Behavioral Assessment rubric for video analysis with specific criteria rated out of a total of 15 indicating risk levels ranging from 1 negligible to very high 6 months
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