Low back pain (LBP) is a highly prevalent and costly condition. In Australia, it is estimated that approximately 4 million people suffer from LBP at any one time (Australian Institute of Health and Welfare, 2004) and the estimates of prevalence around the world range from 22% to 65%, depending on how the condition is defined (Walker, Reference Walker2000). The treatment costs associated with LBP in Australia (a country of 24 million people) are close to $5 billion per annum (Arthritis and Osteoporosis Victoria, 2013). LBP is commonly associated with other important health conditions, and the coexistence of other chronic conditions alongside LBP substantially increases the complexity of the management and care for these patients (Baumeister et al., Reference Baumeister, Knecht and Hutter2012).
Symptoms of insomnia are highly prevalent in patients with LBP. Approximately, 59% of patients with LBP also have significant problems sleeping (Alsaadi et al., Reference Alsaadi, McAuley, Hush and Maher2012), and the coexistence of these conditions is associated with higher levels of pain (Alsaadi et al., Reference Alsaadi, McAuley, Hush and Maher2012), psychological distress, physical disability, fatigue, and daytime sleepiness (McCracken & Iverson, Reference McCracken and Iverson2002). Previous studies have suggested a bidirectional relationship between sleep problems and LBP intensity (Alsaadi et al., Reference Alsaadi, McAuley, Hush, Lo, Bartlett, Grunstein and Maher2014a; Kelly et al., Reference Kelly, Blake, Power, O'Keeffe and Fullen2011). Insomnia is an important predictor of worse prognosis in terms of disability — patients with insomnia and back pain are at higher risk of going onto the disability pension than those without insomnia (Ropponen et al., Reference Ropponen, Silventoinen, Hublin, Svedberg, Koskenvuo and Kaprio2013). Insomnia is also believed to lower pain thresholds and reduce people's mental capacity to deal with pain (Kundermann et al., Reference Kundermann, Krieg, Schreiber and Lautenbacher2004; Novak et al., Reference Novak, Mucsi, Shapiro, Rethelyi and Kopp2004). On the other hand, the experience of pain also affects sleep quality. A previous study found that higher pain intensity during the day was associated with a decrease in the subsequent night's sleep quality (Alsaadi et al., Reference Alsaadi, McAuley, Hush, Lo, Lin, Williams and Maher2014b). Additionally, it is likely that poor sleep quality adversely impacts the management of LBP: the most commonly prescribed treatment by clinicians for patients with LBP — exercise therapy (Freburger et al., Reference Freburger, Carey, Holmes, Wallace, Castel, Darter and Jackman2009) — is likely to be affected by the consequences of insomnia, such as fatigue and daytime sleepiness, potentially leading to worse outcomes. Accordingly, it is plausible that effective management of LBP should address symptoms of insomnia.
The current treatment options for LBP offer only moderate effects at best (Machado et al., Reference Machado, Kamper, Herbert, Maher and McAuley2009). Previous randomized clinical trials have mainly focused on traditional intervention programs targeting specific spinal impairments, such as specific forms of exercise, and have shown limited effects (Ferreira et al., Reference Ferreira, Ferreira, Maher, Herbert and Refshauge2006; Reference Ferreira, Ferreira, Latimer, Herbert, Hodges, Jennings and Refshauge2007). Treatment models focusing on associated comorbidities, such as insomnia, rather than the sole disease or disease-related impairment, have the potential to improve LBP outcomes and in the case of insomnia have not been previously investigated.
Behavioral interventions, such as cognitive behavioral therapy (CBT), are commonly prescribed for insomnia and have been shown to be effective in improving sleep quality (Riemann & Perlis, Reference Riemann and Perlis2009; Trauer et al., Reference Trauer, Qian, Doyle, Rajaratnam and Cunnington2015). Previous studies have investigated the efficacy of CBT for sleep quality for patients with comorbid insomnia and osteoarthritis (Vitiello et al., Reference Vitiello, Rybarczyk, Von Korff and Stepanski2009; Reference Vitiello, McCurry, Shortreed, Baker, Rybarczyk, Keefe and Von Korff2014) or chronic pain (Jungquist et al., Reference Jungquist, O'Brien, Matteson-Rusby, Smith, Pigeon, Xia and Perlis2010; Tang et al., Reference Tang, Lereya, Boulton, Miller, Wolke and Cappuccio2015), and found significant improvements in sleep outcomes as well as in pain and function. However, in these studies patients had to attend face-to-face treatment sessions, a treatment model that incurs high costs and limits the population's accessibility to the intervention. The use of an internet-based CBT program has been found to be effective for improving sleep quality (Espie et al., Reference Espie, Kyle, Williams, Ong, Douglas, Hames and Brown2012; Seyffert et al., Reference Seyffert, Lagisetty, Landgraf, Chopra, Pfeiffer, Conte and Rogers2016) and overcomes the limitations of traditional face-to-face CBT interventions. The employment of an internet-based CBT program for patients suffering from LBP and poor sleep quality has not been previously investigated and has great potential, considering the close relationship between insomnia and LBP.
Although randomized controlled trials are the gold standard design for investigating the effectiveness of an intervention, they do not explicitly take into consideration genetic and familial confounding. Genetic factors have a substantial influence in LBP, with heritability accounting for up to 67% of the variance in liability to LBP as a symptom and with the genetic component being higher for more recurrent and disabling LBP than acute and less disabling LBP (Ferreira et al., Reference Ferreira, Beckenkamp, Maher, Hopper and Ferreira2013). Similarly, genetic factors have been found to be associated with insomnia (Gottlieb et al., Reference Gottlieb, O'Connor and Wilk2007), accounting for at least 33% of the variance of sleep quality, sleep disturbance, and sleep pattern (Barclay et al., Reference Barclay, Eley, Buysse, Rijsdijk and Gregory2010; Heath et al., Reference Heath, Kendler, Eaves and Martin1990; Watson et al., Reference Watson, Harden, Buchwald, Vitiello, Pack, Strachan and Goldberg2014). The randomized co-twin controlled trial design builds on the strengths of traditional trials design as it offers optimal matching to control for confounding, since genetics and a range of environmental variables that might contribute to the response to treatment are accounted for. This design has been successfully used in other areas such as the common cold (Martin et al., Reference Martin, Carr, Oakeshott and Clark1982), and osteoporosis (Hunter et al., Reference Hunter, Major, Arden, Swaminathan, Andrew, MacGregor and Spector2000; Ronkainen et al., Reference Ronkainen, Kovanen, Alen, Pollanen, Palonen, Ankarberg-Lindgren and Sipila2009), but to the best of our knowledge has never been used in LBP.
A randomized co-twin controlled trial investigating the efficacy of a web-based CBT treatment could reveal promising results that could be implemented on a population level. As the proposed study design (a randomized co-twin controlled trial) and intervention (web-based CBT program) are clearly innovative, the aim of this study is to assess the feasibility of this study and determine the optimal approach to conduct a fully powered randomized controlled trial.
The specific aims of this study are to investigate: (1) the rate of recruitment of adult twins registered at the Australian Twin Registry (ATR) with LBP to participate in the trial, (2) the feasibility of data collection and outcome measure completion, (3) contamination of intervention among twins, (4) acceptability and experience of the intervention, and (5) the sample size required for the full trial.
Materials and Methods
Study Design
This is a feasibility study of a randomized co-twin controlled trial with concealed allocation and blinded treatment administrators and trial statistician (Everitt & Howell, Reference Everitt, Howell and Everitt2005). This study has been approved by the Research Ethics Committee of the University of Sydney (2015/386) and been registered at the Australian New Zealand Clinical Trials Registry (ACTRN12615000672550). The protocol has been written following the SPIRIT statement to enhance transparency of content and completeness (Chan et al., Reference Chan, Tetzlaff, Altman, Laupacis, Gotzsche, Krleza-Jeric and Moher2013). The findings of the trial will be reported following the CONSORT statement and the TIDieR checklist (Altman et al., Reference Altman, Schulz, Moher, Egger, Davidoff, Elbourne and Consort2001; Hoffmann et al., Reference Hoffmann, Glasziou, Boutron, Milne, Perera, Moher and Michie2014).
Study Overview
Monozygotic (MZ) and dizygotic (DZ) twins with subacute or chronic LBP will be enrolled. Participants will be randomly assigned to one of two groups and each twin within a pair will receive either a web-based CBT sleep intervention or a control intervention, with randomization taking place within the pair. The intervention will be an interactive web-based sleep intervention based on CBT principles (intervention group), whereas the control intervention will be a web-based education program (control group), with both interventions lasting for 6 weeks. Outcomes will be measured at baseline, immediately post-treatment, and at a 3-month follow-up post-randomization. Participants will be required to answer a questionnaire 1 week after the end of the study containing questions about contamination of intervention. Additionally, twins will answer a telephone interview to investigate their opinion regarding the web-based sleep intervention. All assessment, treatment, and data-collection procedures will be conducted online and all enquiries will be managed electronically or via telephone (Figure 1).
Study design, recruitment process, and flow of participants. Note: ATR = Australian Twin Registry, CBT = cognitive behavioral therapy.
Participants
A total of 30 twins (15 pairs) with current e-mail address in the ATR database and concordant for LBP will be recruited. Twins will be contacted through an e-mail approach coordinated by the ATR. To be included in the study both twins within a pair must meet all of the following criteria:
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1. aged between 18 and 65 years
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2. present with LBP of at least 6 weeks duration and not currently seeking care for their LBP
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3. at least a score of 3 on a 0–10 numerical pain scale (Scrimshaw & Maher, Reference Scrimshaw and Maher2001)
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4. presenting with symptoms of insomnia, based on the DSM-5 criteria for persistent Insomnia disorder (Reynolds et al., Reference Reynolds, Redline and Workgroup2010) assessed by Sleep Condition Indicator (SCI). The SCI is valid, reliable and sensitive to change. The items assess four dimensions: sleep continuity (getting to sleep, remaining asleep); sleep satisfaction (sleep quality, troubled by sleep in general); symptom severity (nights per week, duration of problem); and daytime consequences (personal functioning, daytime performance). The SCI generates scores in the range 0–32, with lower scores indicating worse sleep. A score of ≤16 is indicative of clinically significant insomnia (Espie et al., Reference Espie, Kyle, Hames, Gardani, Fleming and Cape2014). Twins with a score <24 will be included in our study
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5. have current access to the internet with a device with a speaker, such as a computer or tablet.
Participants will be excluded, if they
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1. have a known or suspected serious spinal pathology (fracture, metastatic, inflammatory or infective diseases, and widespread neurological disorder)
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2. had spinal surgery in the past 12 months
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3. are currently using prescribed medication or receiving any other prescribed treatment for insomnia or for depression
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4. are pregnant or lactating women
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5. present with severe or extremely severe symptoms of depression (score >10), anxiety (score >7), and stress (score >12) assessed by the Depression Anxiety Stress Scales (DASS-21; Henry & Crawford, Reference Henry and Crawford2005)
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6. are in ‘poor’ or ‘very poor’ physical or mental health (self-report)
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7. have a diagnosis of substance use disorder (self-report assessed with a question in the screening questionnaire)
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8. are shift workers
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9. have not had their zygosity ascertained.
Recruitment
The ATR will send an invitation e-mail with information about the study to twins registered in the database. At the end of the information sheet, twins will be invited to answer a screening questionnaire. Complete twin pairs meeting all preliminary inclusion criteria will be invited to participate in the study and will receive the participant information statement and informed consent. Only those participants meeting the inclusion criteria and returning the informed consent will be included in the study. The trial coordinator will send the link to the web-based baseline questionnaire for those twins who met the inclusion criteria before randomization.
Randomization
Once both twins in a pair meet these inclusion criteria and agree to participate in the study, they will be randomized into one of two groups: one twin from each pair will be randomly allocated to each of the intervention groups, with randomization taking place within the pair. Allocation will be performed using a computer-generated random allocation schedule operated by a remote researcher and concealed from the main assessor of the study. Both twins within a pair will start the intervention at a synchronized time. Twins enrolled in the trial will be contacted by phone to be advised about their intervention allocation and to receive details about the intervention.
Blinding
Treatment administrators and the trial statistician will be blinded to group allocation. Blinding of participants to the active, experimental intervention will also be attempted. In order to check whether participants are blinded to allocation, at the end of the intervention period, participants will be asked ‘Which intervention did you receive?’, and they will be given two options: real (experimental) intervention or sham (control) intervention (Borkovec & Nau, Reference Borkovec and Nau1972; Smeets et al., Reference Smeets, Beelen, Goossens, Schouten, Knottnerus and Vlaeyen2008). Participants will be asked to rate the credibility of the intervention (measured with the Intervention Credibility Scale) after the first week of intervention.
Sample Size
As the aim of this study is to investigate the feasibility of a future randomized co-twin trial, no sample size estimation was performed (Browne, Reference Browne1995; Thabane et al., Reference Thabane, Ma, Chu, Cheng, Ismaila, Rios and Goldsmith2010). Based on feasibility, we have established our sample size as 30 participants (15 complete twin pairs).
Interventions
Web-based CBT
Participants allocated to this group will receive a web-based CBT course comprised of six online sessions, once per week, with sessions unlocked weekly. The program is highly interactive and the content is delivered by an animated personal therapist (avatar), with automated web and e-mail support developed by Sleepio limited (see https://www.sleepio.com) (Table 1). Previous studies, including a randomized-controlled placebo trial, have shown the effectiveness of this program in improving sleep and associated daytime functioning of adults with insomnia (Espie et al., Reference Espie, Kyle, Williams, Ong, Douglas, Hames and Brown2012). In this web-based program, underlying algorithms feed the delivery of information, support, and advice in a personally tailored manner. Each session has a minimum duration of 20 min. Participants make a time for the session and are prompted via e-mail if they fail to attend the session. Participants are required to complete an electronic daily sleep diary over the intervention period. Each participant has an online case file, comprised of four sections: a progress review, a reminder of strategies to try out between sessions, an agreed sleep schedule, and a list of additional reading. It also includes additional relaxation strategies and advice on lifestyle and bedroom factors (sleep hygiene). Participants will have access to a video library and back catalogue of session content and Wikipedia style articles. Web-based CBT users will also be able to participate in a moderated social network/community of users. The CBT content is consistent with the literature, covering behavioral (e.g., sleep restriction, and stimulus control) and cognitive (e.g., thought restructuring, imagery, articulatory suppression, paradoxical intention, and mindfulness) strategies.
Summary of Interventions
N/A = not applicable.
Control intervention
Participants in the control group will be given a web-based education program delivered by e-mail (Table 1). Participants will receive a weekly e-mail in newsletter format over a 6-week period (to allow for matching with the web-based CBT group), containing material with information regarding sleep, mainly extracted from the Sleepio library. The content of each weekly newsletter will be different, but all participants will receive the same material during the intervention period. This intervention was chosen for the control group because there is evidence that sleep hygiene alone is not effective in the treatment of chronic insomnia (Schutte-Rodin et al., Reference Schutte-Rodin, Broch, Buysse, Dorsey and Sateia2008). Participants randomized to this group will be offered the web-based CBT package free of charge upon completion of the study, in case we find results favouring the intervention group.
Feasibility Outcomes
The main outcomes of this study include aspects related to the feasibility of a randomized co-twin controlled trial investigating a CBT sleep intervention in the treatment of patients with LBP. Records will be kept throughout the study and, in addition, a telephone interview will be used to investigate twins’ opinions regarding the intervention and general aspects of the study. The interview will be conducted with twins who have concluded the study and we will attempt to also interview those who have dropped out. The phone interview will be recorded. Additionally, data on the relationship between the twins, including twin bond, communication, and time living together will also be collected using a questionnaire developed by the ATR. A detailed description of the assessment of each of the feasibility aspects is provided below.
Recruitment rate
Recruitment rate will be recorded during the entire recruitment process. Records will be kept regarding the number of twins screened for entry to the trial. When a twin is not admitted to the trial, the reason why he/she was ineligible for inclusion will be recorded. Similarly, if eligible, the reasons for declining participation in the trial will be noted. Consent rates will also be recorded.
Feasibility of data collection and outcome measure completion
The number of missing items for each questionnaire will be recorded. The number of participants completing the intervention program and answering the follow-up questionnaires will be recorded. The number of participants lost in each phase of the study will be noted and the reasons for dropping out will be recorded when possible. During the phone interview, participants will be asked about their opinion regarding the data collection method (electronic), understanding of study questionnaire and data collection tools, and length of time to complete the questionnaires.
Contamination of intervention
Despite all the advantages in conducting a randomized co-twin trial, contamination of intervention between twins in a pair could be a threat to the methodological quality of the trial. On completion of the study intervention, contamination of intervention will be discussed with participants during the telephone interview, and participants will be asked questions such as how difficult it was not to talk to the co-twin about the intervention (Table 2). To ensure interventions are delivered according to protocol, at the first treatment session twins will be invited to commit (or not) to the course. Twins will be asked not to discuss with their co-twins about the intervention they are receiving.
Contamination of Treatment Questions
Acceptability and experience of intervention
According to the trial protocol, each participant in the experimental and control groups will be required to participate in a web-based program for a period of 6 weeks. All web-based interactions from the participants in the web-based CBT course will be electronically stored and participation activity will be assessed, using the following data: diary entries, session activities, engagement with the community, and adherence to tasks. Twins’ opinions regarding the intervention, including the relevance of the intervention for them, will be investigated during the telephone interview.
Sample size requirement
To the best of our knowledge, this will be the first randomized co-twin controlled trial in LBP and also the first study to investigate an online CBT sleep quality intervention for LBP sufferers. Therefore, the results from this feasibility study will be used to generate data for sample size calculations for the definitive trial. The sample used for this feasibility study is representative of the target study population (twins registered with the ATR). Additionally, if this study proves to be feasible, the same inclusion and exclusion criteria will be used in the definitive trial. The quantitative data generated by this study will be supplemented by qualitative data.
Patient Outcomes
Patient outcomes will be measured at baseline, immediately post-intervention, and at a 3-month follow-up post-randomization. All data will be collected using electronic questionnaires. The patient outcomes will include the following:
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1. pain self-efficacy, measured by the pain self-efficacy questionnaire (PSEQ; Nicholas et al., Reference Nicholas, Wilson and Goyen1992)
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2. function, assessed by the patient-specific functional scale (PSFS; Hall et al., Reference Hall, Maher, Latimer, Ferreira and Costa2011)
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3. average pain intensity over the last week, assessed by a 0–10 pain scale (Scrimshaw & Maher, Reference Scrimshaw and Maher2001)
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4. disability, assessed by the Roland Morris disability questionnaire (Roland & Fairbank, Reference Roland and Fairbank2000)
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5. physical activity level, assessed by the International Physical Activity Questionnaire Short Form (IPAQ-SF; Lee et al., Reference Lee, Macfarlane, Lam and Stewart2011)
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6. insomnia severity, assessed by the insomnia severity index (Bastien et al., Reference Bastien, Vallieres and Morin2001)
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7. subjective sleep efficiency: data obtained from the sleep diary, assessed at baseline, post-intervention and at 3 months post-randomization (Espie et al., Reference Espie, Kyle, Williams, Ong, Douglas, Hames and Brown2012).
Data Integrity
Study data will be collected and managed using REDCap electronic data capture tools hosted at the University of Sydney (Harris et al., Reference Harris, Taylor, Thielke, Payne, Gonzalez and Conde2009). REDCap (Research Electronic Data Capture) is a secure, web-based application designed to support data capture for research studies. Data will be stored in spreadsheets and transferred to appropriate statistical software for analysis by an investigator blinded to group allocation. Spreadsheets will be regularly scrutinized for omissions and errors.
Controlling Bias and Protocol Protection
The design that will be employed in this study includes key methodological features that have been recognized as important to minimize bias in controlled trials: randomization, concealed allocation, specification of eligibility criteria, blinded treatment administrators, and trial statistician. The nature of the treatments precludes blinding of participants, although treatment credibility will be assessed using the Credibility Scale. Participants will not be informed about which components of the treatment are active, and instead they will be informed that they will be randomized to two different web-based programs. Additionally, the co-twin design allows optimal matching to control for confounding, including genetic and environmental factors.
This trial has been registered, and to ensure that the study protocol is followed consistently, all personnel involved in the study will be appropriately trained. The nature of the web-based programs will ensure that all participants receive the same standardized intervention, as per protocol.
Data Analysis
Statistical analysis
Since this is a feasibility study, descriptive statistics will be used to explore the data. Analysis will focus on variability of the data (assessed by confidence intervals) rather than hypothesis testing since it is not powered appropriately to assess statistical significance. Treatment effects will be represented by summary (such as mean), and precision measures (such as confidence interval).
The co-twin design, with randomization taking place within the pair, offers high levels of adjustment and more precise estimates of effects than non-twin trials (Dupont, Reference Dupont1988; Visscher et al., Reference Visscher, Gordon and Neale2008). Therefore, the sample size needed to identify the efficacy of an intervention is believed to be smaller than in a traditional non-twin trial. It is intended that the results of the study will enable determination of the appropriate sample size for a full trial (Thabane et al., Reference Thabane, Ma, Chu, Cheng, Ismaila, Rios and Goldsmith2010). We will explore, through descriptive analysis, trends in treatment effect sizes in twins reporting different levels of symptoms of insomnia. Additionally, we will attempt to investigate any trend in data variability in MZ twins compared to DZ Twins.
The data gathered from the telephone interview will be qualitatively analyzed. Main areas to be explored will be: reasons for participation in the study and for dropping out, relevance of the intervention for them, contamination of intervention, understanding of study questionnaire and data collection tools, twins’ views on the data collection method, and barriers and motivators to participate in the study.
Criteria for Feasibility
Based on the results of this study one of the following decisions will be made: (1) study is not feasible, and therefore should not proceed to full trial; (2) study is feasible, but modifications are required; (3) study is feasible and no modifications are required (Thabane et al., Reference Thabane, Ma, Chu, Cheng, Ismaila, Rios and Goldsmith2010). The results of this feasibility study will be interpreted based on the following criteria to determine whether it is feasible to proceed to the full trial:
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1. Recruitment rate of twins approached by the ATR: 10% recruitment rate considering all twins registered (the ATR currently has over 35,000 twin pairs registered), and at least 70% of all eligible pairs can be included. In case these values are not achieved, the reasons for declining participation will be analyzed and the recruitment approaches will be restructured. Additionally, the communication material used to approach twins will be checked and other methods of collecting data might be necessary, such as paper-based questionnaires, and use of incentives for participating in the study might be needed.
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2. Feasibility of data collection and outcome measures completion: No more than 20% missing data for the outcome measures, and a minimum of 85% follow-up rate, based on the PEDro scale (www.pedro.org.au), will be used as a measure of feasibility of data collection and measure completion. If these targets are not achieved, the information collected during the interview regarding reasons for dropping out, twins’ opinions regarding the method of data collection, understanding of study questionnaire and data collection tools, and amount of time required to answer the questionnaires will be used to modify the protocol.
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3. Contamination of intervention: No more than 15% of twins being aware of the intervention their co-twins were receiving and indicating that they have changed their behavior as a consequence of this knowledge. If we find a contamination rate greater than 15%, strategies to avoid it will be sought. For instance, we aim to explore whether contamination of intervention was associated with the level of bonding between twins, living together, or communication between twins. If these factors affect contamination they could be addressed and considered in the recruitment strategy of the full trial.
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4. Acceptability and experience of intervention: Adherence rate of 75%, based on the results of a previous study using Sleepio (Espie et al., Reference Espie, Kyle, Williams, Ong, Douglas, Hames and Brown2012). The information collected during the phone interview regarding the twins’ opinions in relation to the intervention will be used to support the interpretation of these results and to establish strategies to increase attendance rate.
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5. Sample size requirement: Caution will be used when calculating the sample size required for the full trial, as results from feasibility studies can potentially mislead sample size calculation (Thabane et al., Reference Thabane, Ma, Chu, Cheng, Ismaila, Rios and Goldsmith2010). To avoid generating misleading results, we will supplement the information with qualitative data.
The criteria for the full study to be considered feasible or for requiring modification have been established above. The following criteria will be used for considering the study as not feasible: no apparent change in the outcomes with confidence intervals that include large negative values, or when the established criteria have not been met and no strategies can be used to overcome the issues (Thabane et al., Reference Thabane, Ma, Chu, Cheng, Ismaila, Rios and Goldsmith2010).
Discussion
There are many aspects of this trial that are innovative, such as investigation of an intervention approach that has not been tested in the target population (people with LBP) and the twin design. Therefore, the investigation of the feasibility of the study is imperative before planning the full trial, including such pioneering aspects.
This feasibility study includes specific and clear feasibility objectives, and clear analytic plans, and explicit criteria have been established to assess the feasibility of the full study. If this study is considered feasible in the current format, the same design and methods will be used for the full study. However, if modifications are required, they will be conducted according to the information collected in this feasibility study. This will ensure the quality and efficiency of the full trial. In the case that the study is considered as not feasible, the full study will not be conducted, saving resources that otherwise would be spent unnecessarily.
This study will represent a major advance in the field because symptoms of insomnia are strongly associated with chronic LBP and other musculoskeletal conditions, and the use of a co-twin design has the potential to provide precise estimates of treatment effects in LBP. Results will have a substantial impact in the identification of a new intervention that could be directly translated into the management of LBP.
This study will investigate the feasibility of a randomized co-twin trial investigating the efficacy of a web-based CBT program for insomnia to improve sleep and LBP outcomes in people with subacute or chronic LBP and symptoms of insomnia. Our findings will inform the preliminary efficacy of a sleep intervention for LBP, and the feasibility of conducting a definitive randomized co-twin trial.
Acknowledgments
Sleepio Limited for providing the web-based CBT intervention. The Australian Twins Registry for their assistance in the recruitment process. Trial registration: Australian New Zealand Clinical Trials Registry: ACTRN12615000672550. This research received no specific grant from any funding agency, commercial or not-for-profit sectors. MLF is supported by Sydney Medical Foundation/Sydney Medical School.
Conflicts of Interests
None
Details of Ethical Approval
The authors assert that all procedures contributing to this work comply with the ethical standard of the relevant national and institutional committees on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008.
