Department of Health Sciences/ Mental Health, Activity and Participation (MAP), Lund University, Box 157, SE-22100, Lund, Sweden.
Department of Clinical Science/Psychiatry, Umeå University, SE-90185, Umeå, Sweden.
BMC Psychiatry. 2017 Nov 9;17(1):363. doi: 10.1186/s12888-017-1524-7.
BACKGROUND: Many with a mental illness have an impoverished everyday life with few meaningful activities and a sedentary lifestyle. The study aim was to evaluate the effectiveness of the 16-week Balancing Everyday Life (BEL) program, compared to care as usual (CAU), for people with mental illness in specialized and community-based psychiatric services. The main outcomes concerned different aspects of subjectively evaluated everyday activities, in terms of the engagement and satisfaction they bring, balance among activities, and activity level. Secondary outcomes pertained to various facets of well-being and functioning. It was hypothesized that those who received the BEL intervention would improve more than the comparison group regarding activity, well-being and functioning outcomes. METHODS: BEL is a group and activity-based lifestyle intervention. CAU entailed active support, mainly standard occupational therapy. The BEL group included 133 participants and the CAU group 93. They completed self-report questionnaires targeting activity and well-being on three occasions - at baseline, after completed intervention (at 16 weeks) and at a six-month follow-up. A research assistant rated the participants' level of functioning and symptom severity on the same occasions. Non-parametric statistics were used since these instruments produced ordinal data. RESULTS: The BEL group improved more than the CAU group from baseline to 16 weeks on primary outcomes in terms of activity engagement (p < 0.001), activity level (p = 0.036) and activity balance (p < 0.042). The BEL group also improved more on the secondary outcomes of symptom severity (p < 0.018) and level of functioning (p < 0.046) from baseline to 16 weeks, but not on well-being. High intra-class correlations (0.12-0.22) indicated clustering effects for symptom severity and level of functioning. The group differences on activity engagement (p = 0.001) and activity level (p = 0.007) remained at the follow-up. The BEL group also improved their well-being (quality of life) more than the CAU group from baseline to the follow-up (p = 0.049). No differences were found at that time for activity balance, level of functioning and symptom severity. CONCLUSION: The BEL program was effective compared to CAU in terms of activity engagement. Their improvements were not, however, greater concerning other subjective perceptions, such as satisfaction with daily activities and self-rated health, and clustering effects lowered the dependability regarding findings of improvements on symptoms and functioning. Although the CAU group had "caught up" at the follow-up, the BEL group had improved more on general quality of life. BEL appeared to be important in shortening the time required for participants to develop their engagement in activity and in attaining improved quality of life in a follow-up perspective. TRIAL REGISTRATION: The study was registered with ClinicalTrial.gov. Reg. No. NCT02619318 .
背景:许多患有精神疾病的人日常生活贫困,几乎没有有意义的活动,生活方式久坐不动。本研究旨在评估为期 16 周的平衡日常生活(BEL)计划与常规护理(CAU)相比,对专门和社区精神科服务中的精神疾病患者的有效性。主要结果涉及主观评估日常生活活动的不同方面,包括参与度和满意度、活动平衡和活动水平。次要结果涉及各种福祉和功能方面。假设接受 BEL 干预的人在活动、福祉和功能方面的改善会超过对照组。
方法:BEL 是一种基于小组和活动的生活方式干预。CAU 包括主动支持,主要是标准职业治疗。BEL 组包括 133 名参与者,CAU 组包括 93 名参与者。他们在三个时间点完成了针对活动和福祉的自我报告问卷——基线、完成干预后(16 周)和 6 个月随访。研究助理在相同的时间点评估参与者的功能水平和症状严重程度。由于这些工具产生了有序数据,因此使用了非参数统计。
结果:与 CAU 相比,BEL 组从基线到 16 周在活动参与度(p<0.001)、活动水平(p=0.036)和活动平衡(p<0.042)方面的主要结果有更大的改善。BEL 组在症状严重程度(p<0.018)和功能水平(p<0.046)方面也从基线到 16 周有更大的改善,但在幸福感方面没有改善。高组内相关系数(0.12-0.22)表明症状严重程度和功能水平存在聚类效应。活动参与度(p=0.001)和活动水平(p=0.007)的组间差异在随访时仍然存在。BEL 组在幸福感(生活质量)方面的改善也比 CAU 组从基线到随访时更大(p=0.049)。当时,活动平衡、功能水平和症状严重程度没有差异。
结论:与 CAU 相比,BEL 计划在活动参与度方面更为有效。然而,他们在其他主观认知方面的改善并不明显,例如对日常活动和自我评估健康的满意度,并且聚类效应降低了对症状和功能改善的发现的可靠性。尽管 CAU 组在随访时“迎头赶上”,但 BEL 组在总体生活质量方面的改善更多。BEL 似乎在缩短参与者发展活动参与度和实现随访时改善生活质量所需的时间方面发挥了重要作用。
试验注册:该研究在 ClinicalTrials.gov 上注册。注册号 NCT02619318。
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