| Literature DB >> 32411374 |
Svein O Tjøsvoll1, Paul J Mork2, Vegard M Iversen2, Marit B Rise3, Marius S Fimland1,4.
Abstract
BACKGROUND: We investigated the feasibility of a 16-week supervised heavy resistance training program with weekly undulating periodization for individuals with persistent non-specific low-back pain (LBP).Entities:
Keywords: Feasibility study; Heavy resistance training; Mixed methods; Muscle strength; Numeric pain rating scale; Pain self-efficacy; Pain-related disability; Persistent non-specific low back pain; Weekly undulating periodization
Year: 2020 PMID: 32411374 PMCID: PMC7206666 DOI: 10.1186/s13102-020-00181-0
Source DB: PubMed Journal: BMC Sports Sci Med Rehabil ISSN: 2052-1847
Overview of testing, questionnaires, and strength training throughout the 16 weeks’ intervention period
| Week | Tests | Questionnaire | Training emphasis | Set and reps | Pause between sets (min) | % of 1RM |
|---|---|---|---|---|---|---|
| 1 | Baseline test | NPRS, ODI, PSEQ, FABQ, SNQ | Adaptation | 3 x 10 | 1 – 2 | 50 |
| 2 | Adaptation | 3 x 10 | 1 – 2 | 50 | ||
| 3 | Adaptation | 3 x 10 | 1 – 2 | 50 | ||
| 4 | Pretest 1RM | Adaptation | 3 x 10 | 1 – 2 | 50 | |
| 5 | Strength endurance | 3 x 12 | 1 – 2 | 70 | ||
| 6 | Strength | 3 x 8 | 2 | 80 | ||
| 7 | Strength | 3 x 4 | 3 | 90 | ||
| 8 | Midtest 1RM | NPRS, ODI, PSEQ | Deload | 3 x 10 | 1 – 2 | 50 |
| 9 | Strength endurance | 3 x 12 | 1 – 2 | 70 | ||
| 10 | Strength | 3 x 8 | 2 | 80 | ||
| 11 | Strength | 3 x 4 | 3 | 90 | ||
| 12 | Deload | 3 x 10 | 1 – 2 | 50 | ||
| 13 | Strength endurance | 3 x 12 | 1 – 2 | 70 | ||
| 14 | Strength | 3 x 8 | 2 | 80 | ||
| 15 | Qualitative Focus group interviews | Strength | 3 x 4 | 3 | 90 | |
| 16 | Posttest 1RM | NRPS, ODI, PSEQ | Deload | 3 x 10 | 1 – 2 | 50 |
Abbreviations: NPRS Numerical Pain Rating Scale, ODI Oswestry Low Back Disability Questionnaire, PSEQ Pain Self- Efficacy Questionnaire, FABQ Fear- Avoidance Beliefs Questionnaire, 1RM 1 Repetition maximum, SNQ Standardized Nordic Questionnaire.
Fig. 1Participant flow throughout the study
Baseline characteristics of participants
| Participants characteristics | ( |
|---|---|
| Age, mean (SD) | 40 (13) |
| Women, % | 45.8 |
| Married or cohabitant, % | 83 |
| Education (High school, college, university), % | 100 |
| Employed (full-time or part time), % | 87.5 |
| Sick leave (fully/partially), % | 0 |
| Pain has prevented you from doing leisure time activities, % | 70.8 |
| Neck pain, % | 50 |
| Shoulder pain, % | 33 |
| Hip pain, % | 29 |
| Upper back pain, % | 8 |
| Knee pain, % | 8 |
| Fear avoidance beliefs questionnaire | |
| Part A – Activity beliefs (0–24), mean (SD) | 8.1 (5) |
| Part B – Work beliefs (0–42), mean (SD) | 9.8 (6.2) |
Abbreviations: SD Standard deviation, LBP Low back pain
Intention to treat analysis of outcomes, estimated means and 95% confidence intervals at baseline, 8 weeks and 16 weeks
| Outcome | Baseline | 8 weeks | 16 weeks | Effect size (Baseline to 16 weeks) |
|---|---|---|---|---|
| Outcomes | Mean (95% CI) | Mean (95% CI) | Mean (95% CI) | Cohens d |
| LBP (NPRS; 0–10) | ||||
| Current | 3.1 (2.5–3.7) | 1.8 (1.2–2.4)* | 1.7 (1.1–2.4)* | 1.0 (0.5–1.4) |
| Worst last 2 weeks | 6.5 (5.8–7.1) | 3.8 (3.1–4.5)** | 3.0 (2.3–3.7)** | 2.1 (1.6–2.7) |
| Worst last 4 weeks | 6.7 (6.1–7.4) | 4.2 (3.5–4.9)** | 3.5 (2.8–4.2)** | 2.1 (1.5–2.6) |
| ODI (0–50) | 9.2 (7.9–10.5) | 7.0 (5.7–8.3)* | 5.3 (3.9–6.7)* | 1.2 (0.8–1.7) |
| PSEQ (0–60) | 48.8 (46.2–51.4) | 54.3 (51.7–57.3)* | 56.5 (53.8–59.2)* | 1.2 (0.9–1.6) |
| Squat (kg) | 67.8 (58.8–76.8) | 84.9 (75.9–93.9)** | 103.2 (94.2–112.3)** | 1.7 (1.6–1.9) |
| Bench – press (kg) | 56.9 (47.6–66.2) | 64.4 (55.1–73.7)** | 74 (64.7–83.4)** | 0.8 (0.7–0.9) |
| Deadlift (kg) | 77.6 (68.5–86.7) | 93.6 (84.4–102.7)** | 105.3 (96.7–114.6)** | 1.3 (1.1–1.6) |
| Pendlay row (kg) | 49.9 (43.2–56.7) | 55.8 (49.1–62.6)** | 62.7 (55.9–69.4)** | 0.8 (0.7–0.9) |
Abbreviations: NPRS Numerical Pain Rating Scale, ODI Oswestry Low Back Disability Questionnaire, PSEQ Pain Self- Efficacy Questionnaire, LBP Low Back Pain, CI Confidence Interval. Change from baseline* p ≤ 0.05, ** p ≤ 0.01
Per protocol analysis (participation > 70) of outcomes, estimated means and 95% confidence intervals from baseline to 8 and 16 weeks
| Outcome | Baseline | 8 weeks | 16 weeks | Effect size (Baseline to 16 weeks) |
|---|---|---|---|---|
| Outcomes | Mean (95% CI) | Mean (95% CI) | Mean (95% CI) | Cohens d |
| LBP (NPRS; 0–10) | ||||
| Current | 2.9 (2.2–3.6) | 1.9 (1.2–2.5)* | 1.8 (1.1–2.4)* | 0.81 (0.3–1.3) |
| Worst last 2 weeks | 6.5 (5.8–7.2) | 3.9 (3.1–4.6)** | 3.0 (2.3–3.8)** | 2.1 (1.6–2.7) |
| Worst last 4 weeks | 6.7 (6.2–7.5) | 4.3 (3.5–5.7)** | 3.6 (2.8–4.3)** | 2.0 (1.5–2.6) |
| ODI (0–50) | 8.4 (7.8–9.7) | 7.3 (5.9–8.6)* | 5.3 (3.9–6.6)* | 1.1 (0.7–1.5) |
| PSEQ (0–60) | 49.1 (51.3–57.1) | 54.2 (51.3–57.1)* | 56.1 (53.2–59.6)* | 1.1 (0.8–1.5) |
| Squat strength (kg) | 65.4 (55.8–75.0) | 82.1 (72.5–91.7)** | 100.4 (90.7–110.3)** | 1.7 (1.6–1.9) |
| Bench – press (kg) | 54.7 (44.4–65.6) | 62.4 (51.7–72.3)** | 71.7 (61.4–82.1)** | 0.8 (0.7–0.9) |
| Deadlift (kg) | 76.4 (66.5–86.8) | 92.9 (82.4–103.3)** | 104.7 (94.2–115.2)** | 1.3 (1.0–1.5) |
| Pendlay row (kg) | 48.3 (41.9–55.7) | 53.6 (46.3–61.0)** | 60.5 (53.1–67.8)** | 0.8 (0.7–0.9) |
Abbreviations: NPRS Numerical Pain Rating Scale, ODI Oswestry Low Back Disability Questionnaire, PSEQ Pain Self- Efficacy Questionnaire, LBP Low Back Pain, CI Confidence Interval. Change from baseline* p ≤ 0.05, ** p ≤ 0.01