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Clinical RelevanceDOI 4 min read
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Patient-friendly summary

If you read nothing else

For people with chronic pain who sleep poorly, a structured insomnia therapy called CBT-I is the most promising way to improve sleep, at least in the short term.

Bottom line

Cognitive behavioural therapy for insomnia (CBT-I) is an effective treatment to improve sleep quality in people with chronic pain post-treatment, but the benefit weakens over time and effects on pain, quality of life and mood are limited; sleep hygiene alone is not effective, and most other interventions lack sufficient evidence.

Moderate evidence

Published

2022
4 years ago
Recent

Evidence hierarchy

Meta-analysis
Systematic Review ◀ this study
RCT
Cohort
Case-Control
Case Report
Expert Opinion

Study participants

3346 participants across 42 randomised trialsStudy mean ages ranged from 31 to 73 years (average 51 years)Not reported

Adults aged 18 and older with chronic non-cancer pain (conditions including fibromyalgia, osteoarthritis, rheumatoid arthritis, back/neck pain, multiple sclerosis and migraine)

Full research — for clinicians and curious readers

Study Summary

This systematic review and meta-analysis evaluated non-pharmacological, non-invasive interventions to improve sleep in adults with chronic non-cancer pain. Across 42 randomised trials involving 3346 participants, cognitive behavioural therapy for insomnia (CBT-I) showed the strongest evidence, improving sleep quality post-treatment compared with controls (SMD -1.23, 95% CI -1.76 to -0.70). The benefit was reduced but persisted at 3 and 6 months, while improvements in pain, anxiety and depression were generally not sustained long-term. Sleep hygiene alone did not improve sleep, and many other interventions had too few studies to draw conclusions.

74/100
Evidence StrengthStrong
Study Quality
Sample Size
Replication

Key Findings

FindingDetailImpact
CBT-I improved sleep quality after treatmentIn 9 studies with 385 participants, CBT-I improved questionnaire-assessed sleep quality versus untreated controls post-treatment, SMD -1.23 (95% CI -1.76 to -0.70; p<0.00001), though heterogeneity was high (I2 80%). In 3 studies at low risk of bias the effect was only slightly reduced, SMD -1.01 (95% CI -1.79 to -0.22; p=0.01).High
Sleep benefit weakened over time but still favoured CBT-IThe difference between groups was lower at 3 and 6 months after treatment but still favoured CBT-I over control. Most studies had follow-up of 3 months or less; only 9 studies reported 6-month and 2 studies reported 12-month outcomes.Medium
Pain, anxiety and depression reductions after CBT-I were modest and not durablePain was reduced post-treatment (9 studies, 370 people, SMD -0.24, 95% CI -0.45 to -0.03; p=0.02) but not in the 3 low-risk-of-bias studies and not sustained at 3 months or longer. Anxiety (SMD -0.54, 95% CI -1.01 to -0.06; p=0.03) and depression (SMD -0.57, 95% CI -1.05 to -0.08; p=0.08) showed post-treatment benefit, but longer-term evidence was lacking.Medium
CBT-I outperformed sleep hygiene; sleep hygiene alone showed no benefitWhen the study at unclear risk of bias was excluded, CBT-I improved sleep quality versus sleep hygiene (SMD -0.53, 95% CI -0.94 to -0.12; p=0.01) and pain in the 2 low-risk studies (SMD -0.85, 95% CI -1.26 to -0.43; p<0.0001). Sleep hygiene compared with untreated controls showed no benefit for sleep quality or pain.High
Other interventions had insufficient evidence to draw conclusionsMindfulness showed a small post-treatment sleep-quality benefit (SMD -0.41, 95% CI -0.72 to -0.11; p=0.008), while exercise, Tai Ji Quan, hydrotherapy, manual therapy, acupressure, reflexology, bright light, transcranial stimulation and mattress interventions were each evaluated in small numbers of studies with insufficient evidence.Medium
Adverse events were rarely and inconsistently reportedOnly 9 of 42 studies reported adverse-event data, and no serious adverse events were reported. Reported events were minor (e.g., rash from wearing an actigraph, tenderness at a testing site, pain exacerbation, chlorine hypersensitivity).Low
Study Methodology
Study Design
Systematic review and random-effects meta-analysis of randomised controlled trials, registered with PROSPERO (CRD42019093799) and reported per PRISMA; risk of bias assessed with the Cochrane tool
Sample Size
42 randomised trials with 3346 participants randomised to 94 groups (56 groups received a sleep-targeting intervention)
Duration
Databases searched from inception to 8 April 2020; trial follow-up assessed post-treatment and at 3 and 6 months where reported (15 studies reported follow-up at 3 months or longer; 9 at 6 months; 2 at 12 months)
Population
Adults aged 18 years or older with chronic non-cancer pain (mean ages across studies 31 to 73 years; average 51 years); conditions included fibromyalgia, osteoarthritis, rheumatoid arthritis, spinal/low back and neck pain, multiple sclerosis and migraine
Outcome Measures
Sleep quality and duration (questionnaires, sleep diaries, actigraphy, polysomnography; e.g., sleep latency, sleep efficiency, wake after sleep onset, total sleep time, awakenings, Epworth Sleepiness Scale) · Pain · Health-related quality of life · Psychological wellbeing (anxiety, depression) · Adverse events

Strengths

  • Robust, systematic methodology following Cochrane guidance with PROSPERO pre-registration and PRISMA reporting
  • Comprehensive search across five databases with no language restrictions and dual independent screening and data extraction
  • Large evidence base of 42 RCTs (3346 participants) spanning multiple chronic pain conditions
  • Risk-of-bias sensitivity analyses applied, with effects confirmed in low-risk-of-bias subsets for the main CBT-I finding

Limitations

  • High statistical heterogeneity in several meta-analyses (e.g., I2 80% for the main CBT-I sleep-quality analysis)
  • Many interventions were evaluated in only small numbers of studies, limiting opportunity for meta-analysis and firm conclusions
  • Highly heterogeneous secondary outcome measures (especially for quality of life and psychological wellbeing) limited comparison between studies
  • Most trials had follow-up of 3 months or less, so longer-term effectiveness remains unclear
  • The chronic pain population was clinically heterogeneous, and adverse-event reporting was inconsistent (only 9 of 42 studies)

Key Takeaways for Patients

What This Means for You

  1. About two thirds of people with chronic pain report problems sleeping, and sleep and pain influence each other in both directions.

  2. Cognitive behavioural therapy for insomnia (CBT-I) has the strongest evidence for improving sleep quality in people with chronic pain, at least in the short term.

  3. The sleep benefit tends to weaken over the following months, and improvements in pain and mood were modest and often not lasting in this review.

  4. Sleep hygiene advice on its own did not improve sleep in these studies and appeared less effective than CBT-I.

  5. Many other approaches (such as mindfulness, exercise, hydrotherapy and manual therapy) have been tried but were studied too little to know if they reliably help sleep.

Read the Full Paper

Access the complete peer-reviewed study from BMC Musculoskeletal Disorders

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