Study Design and Participants
We conducted a randomized clinical trial with parallel groups. The trial compared I-MORE to the less comprehensive O-ACT for individuals on sick leave due to musculoskeletal or common mental disorders. The primary outcome was sickness absence during 12 months of follow-up [10]. The study protocol and several other studies have been published from this project, and the description of the methods are partly overlapping with previous studies [10, 17,18,19,20,21]. The study was approved by the Regional Committee for Medical and Health Research Ethics in Central Norway (No.: 2012/1241) and is registered in clinicaltrials.gov (No.: NCT01926574). The results are presented according to the CONSORT statement [22].
Eligible participants were 18 to 60 years of age who at inclusion had been sick listed 2 to 12 months with a diagnosis within the musculoskeletal (L), psychological (P) or general and unspecified (A) chapters of the ICPC-2 (International Classification of Primary Care, Second edition). Sick leave status had to be at least 50% off work at inclusion. Exclusion criteria, assessed by a comprehensive questionnaire and an outpatient screening performed by a physician, a physiotherapist and a psychologist, were: (1) alcohol or drug abuse; (2) serious somatic (e.g. cancer, unstable heart disease) or psychological disorders (e.g. high suicidal risk, psychosis, ongoing manic episode); (3) specific disorders requiring specialized treatment; (4) pregnancy; (5) currently participating in another treatment or rehabilitation program; (6) insufficient oral or written Norwegian language skills to participate in group sessions and fill out questionnaires; (7) scheduled for surgery within the next 6 months; and (8) serious problems with functioning in a group setting, as assessed by the multidisciplinary clinical team.
The Rehabilitation Programs
I-MORE consisted of several components; group-based ACT, a form of cognitive behavioral therapy, individual and group-based physical training, mindfulness, education on various topics, and individual meetings with the coordinators in work-related problem-solving sessions including creating a RTW-plan. Table 1 shows an overview of the content of the program. A more detailed description can be found in the study protocol article [17]. A certified ACT-instructor supervised the coordinators who mentored the participants, both before and on a monthly basis during the intervention. ACT was chosen as the cognitive behavioral therapy approach in this study because of its applicability across diagnostic groups [12]. The program lasted 3.5 weeks with 6–7 h each day except on weekends. It took place at Hysnes rehabilitation center, which was established as a part of St. Olavs Hospital in central Norway.
Table 1 Overview of the two interventions O-ACT consisted mainly of group-based ACT once a week for 6 weeks, each session lasting 2.5 h. The sessions were held at the Department of Physical Medicine and Rehabilitation, St. Olavs Hospital, and was led by one of two physicians or a psychologist, all supervised by the same ACT-instructor as in I-MORE. The participants were given home assignments between sessions, including a daily 15 min audio-guided mindfulness practice. In addition, the participants were offered two individual sessions with a social worker experienced in occupational rehabilitation and trained in ACT to clarify personal values and work-related issues. The program also included a motivational group discussion with a physiotherapist on the benefits of physical training. One individual session with both the social worker and group leader present ended the program. In this session, a summary letter was written to the participant’s general practitioner. A more detailed description of the programs has been published elsewhere [10, 17].
Study Context
All legal residents in Norway are included in the Norwegian public insurance system. Medically certified sick leave is compensated with 100% coverage for the first 12 months, with some limitations regarding the size of the salary. The first 16 days are covered by the employer, the rest by the Norwegian Welfare and Labour Administration. After 12 months of sick leave, it is possible to apply for the more long-term medical benefits, work assessment allowance and disability pension, which both covers approximately 66% of the income. Individuals on work assessment allowance are supposed to work according to their work capacity.
Outcome Measures
Sick leave data were obtained from the Norwegian National Social Security System Registry, where all individuals receiving any form of sickness or disability benefits in Norway are registered by their social security number. Based on information from the different medical benefits (sick-leave payments, work assessment allowance and disability pension) we calculated the equivalent of full workdays on medical benefits according to a 5-day workweek for every month during follow-up [19].
Two work participation parameters were calculated: (1) cumulated number of workdays on medical benefits from inclusion to 2-years of follow-up, and (2) time until full sustainable RTW defined as 1 month without sick leave relapse, i.e. first full month without medical benefits (disregarding any graded disability the participant had when entering the study).
Other variables registered by questionnaires at inclusion were anxiety and depression symptoms measured by The Hospital Anxiety and Depression scale (HADS) [23], pain measured by one question from the Brief Pain Inventory (BPI) [24] and level of education, dichotomized as high (college/university) or low.
Randomization and Blinding
Potential participants were identified in the National Social Security System, between October 2012 and November 2014, and invited through a letter. Invited participants completed a short eligibility questionnaire. Those eligible were invited for the outpatient screening assessment. If the screening was passed (Fig. 1), participants were randomized to either I-MORE or O-ACT. A flexibly weighted randomization procedure was provided by the Unit of Applied Clinical Research (third-party) at the Norwegian University of Science and Technology (NTNU) to ensure that the rehabilitation center had enough participants to run monthly groups in periods of low recruitment. As a third party performed the procedure, the randomization was concealed for the researchers and participants.
It was not possible to blind neither the participants nor the caregivers for treatment. Sickness absence data was provided by employees at the Norwegian Welfare and Labor Service, who were unaware of group allocation. The researchers were not blinded.
Statistical Analysis
Sample size was calculated based on the primary outcome, i.e. number of sickness absence days during 12 months of follow-up [10], resulting in 80 persons in each arm. Details about the estimations are published elsewhere [17].
Number of days on medical benefits from inclusion to 2-years of follow-up were calculated and compared using the Mann–Whitney U (Wilcoxon rank sum) test, as sick leave days were not normally distributed. Number of participants in the two groups who received more long-term benefits (work assessment allowance and disability pension) were compared using Pearson χ2 test and the Suissa-Shuster test [25, 26] for expected cell counts over and under 5 respectively. Logistic regression was used to calculate the odds ratio for receiving work assessment allowance at 2-years of follow-up. We performed the analyses both without adjustments and adjusted for gender, age, level of education, main diagnosis for sick leave and length of sick leave at inclusion. Education was dichotomized as high (university college or university) or low. For time until sustainable RTW, Kaplan Meier curves were estimated and compared with the log rank test. We estimated hazard ratios for RTW using Cox proportional hazard model with the Efron method for ties [27]. Time was calculated as number of months and participants were censored at “full sustainable RTW” or end of follow-up. We performed analyses both without adjustment and with adjustment for gender, age, level of education, main diagnosis for sick leave and length of sick leave at inclusion. The proportionality hazard assumption was checked using the Schoenfeld Residual test [28]. All analyses were performed after the intention-to-treat principle, i.e. participants were included in the analyses by their group assignment at randomization.
p-values (two-tailed) < 0.05 were considered statistically significant. Estimate precisions were assessed by 95% confidence intervals. All analyses were done using STATA 14.1 (StataCorp. 2015. Stata Statistical Software: Release 14. College Station, TX: StataCorp LP).