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N/A N=27 Randomized Single-blind Treatment

Reducing Sedentary Behavior to Decrease Low Back Pain: Stand Back Study

Chronic Low Back Pain

Enrolled (actual)
27
Serious AEs
0.0%
Results posted
Feb 2019
Primary outcome: Primary: Low Back Pain Disability — 12.1; 19.6 Oswestry Disability %

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Intervention (Behavioral); No intervention (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of Pittsburgh
Primary completion
Dec 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Low Back Pain Disability
12.1; 19.6
PRIMARY
Usual Low Back Pain
2.87; 3.02
SECONDARY
Quality of Life (Self-reported)
73.33; 62.08
SECONDARY
Mood
87.25; 102.67
SECONDARY
50-ft Walk Test
10.67; 11.09
SECONDARY
Chair Stand Test
10.05; 10.42
SECONDARY
Timed up and go Test
7.49; 8.20
SECONDARY
Unloaded Reach Test
36.2; 34.0
SECONDARY
Presenteeism
27.83; 25.08
SECONDARY
Work Productivity
6.57; 6.61
SECONDARY
Physical Activity
300; 195
SECONDARY
Sedentary Behavior
7.3; 9.0

Summary

This study will test the effects of a sedentary behavior intervention on low back pain in working adults. The behavioral intervention will include the use of a sit-stand desk and a wrist-worn activity prompter that will notify participants when they have been sedentary for too long.

Eligibility Criteria

Inclusion Criteria

  • Have chronic low back pain defined as a back pain problem that has persisted at least 3 months and has resulted in pain on at least half the days in the past 6 months
  • Oswestry low back pain index >20% to ensure a moderate level of disability is present, thus minimizing a potential floor effect
  • Currently perform deskwork at least 20 hours per week at a desk compatible with the sit-stand attachment
  • Stable employment (at least 3 months at current job and plan to stay at current job for the next 6 months)
  • Ability to obtain approval to install sit-stand workstation (i.e., from supervisor)
  • Access to internet connection and email to complete assessment surveys

Exclusion Criteria

  • Unable to provide informed consent
  • Cardiovascular event in the last 6 months (e.g. heart attack, stoke, heart failure, revascularization procedure)
  • Presence of a comorbid condition that would limit ability to reduce sedentary behavior (e.g. currently undergoing treatment for cancer)
  • Back surgery in the past 3 months or planned in the next year
  • Presence of a medical "red flag" for a serious spinal condition (cancer, compression fracture, signs or symptoms of root compression, infection)
  • Inability to tolerate standing for any reason
  • Currently using a sit-stand desk, standing desk, or wearable activity monitor
  • Currently pregnant or planned pregnancy in the next 6 months
  • Blood pressure >159/100 mmHg
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02624687). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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