Protocol and registration
This protocol has been registered with the PROSPERO international prospective register of systematic reviews (registration number: CRD42015025066) and was reported adhering to the Preferred Reporting Items for Systematic Review and Meta-Analysis Protocols (PRISMA-P) 2015 statement [33, 34] (see Additional file 1). The final review will be reported following the Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) statement and the equity extension of the PRISMA statement, PRISMA-E 2012 [35–38]. Important protocol amendments will be documented and published with the results of the review.
Study selection criteria
Types of studies
This systematic review will include published peer-reviewed journal articles from 2005 to July 2015, written in English or German language. Randomized controlled trials (RCTs), which are often considered the gold standard when assessing the effectiveness of interventions, are likely to be less frequently conducted in the field of public health and health promotion . Especially for environmental or policy level interventions, RCTs are rarely available . Therefore, the review will include all types of quantitative experimental as well as observational study designs (with or without concurrent control group) which evaluated the effects of interventions on physical activity among older adults, such as RCTs, cluster randomized controlled trials (cluster RCTs), non-randomized controlled trials (NRCTs), controlled before-and-after (CBA) studies, cohort studies, interrupted-time-series (ITS) studies, or before-and-after (BA) studies. Studies using a cross-sectional design, for example, for evaluating the effects of an intervention in the outdoor environment by comparing the intervention area with a reference area, will also be eligible.
Types of participants
Studies will be included if the study population comprises people aged 50 years and over. Only studies on interventions that potentially address everyone across the social spectrum (universal interventions) will be included.
Thus, studies in which the study population is restricted to particular social groups of older adults (e.g., studies targeted at women or men or at low SES population groups only) will be excluded. Studies whose study participants are restricted with regard to actual physical activity behavior (e.g., study population is described as “inactive", “insufficiently active", “sedentary", “physically active”), functional status (e.g., study population is described as “sarcopenic", “home-bound", “fall-prone", “functionally impaired", “frail”) or specific underlying medical conditions (e.g., dementia, cancer, depression, multiple sclerosis, diabetes) will also be excluded. Furthermore, studies whose study populations are restricted to overweight or obese individuals as well as studies focused on participants receiving nursing or rehabilitation care will not be included.
Studies in which participants met one or more of the abovementioned conditions, but have not been recruited specifically due to these conditions, will be included. Additionally, eligible studies have to report baseline characteristics of participants stratified by at least one social factor according to the PROGRESS-Plus framework. Since only studies focused on older adults will be included in the review, age alone will not be considered as sufficient to fulfill this inclusion criterion.
Types of interventions
Studies will be included if they evaluate the effects of interventions on physical activity behavior among older adults either as the study’s main objective or within a comprehensive intervention design with multiple intervention components. Eligible interventions may operate at various levels (i.e., individual, community, or societal level interventions) and may be delivered in a variety of modes (e.g., face-to-face, phone call, online, smartphone, changes to the built environment) with various frequency, duration, or intensity characteristics. No restrictions on intervention and follow-up duration will be applied.
Types of comparators
The review will include quantitative study designs with and without concurrent control groups. Therefore, where applicable, controls may be active (i.e., receiving an alternative intervention approach) or passive (e.g., receiving no intervention, usual care, or waitlist control group). Studies which compare the effects of an intervention between residents of two areas, in one of which an intervention was implemented, will also be eligible.
Types of outcome measures
To be included in the review, studies have to report changes in physical activity, either assessed objectively (e.g., by pedometers or accelerometers) or subjectively (e.g., by questionnaires). Studies only measuring changes in psychological outcomes (e.g., intentions, self-efficacy, knowledge, attitudes) regarding physical activity instead of changes in physical activity behavior itself will be excluded. Furthermore, studies in which effects on physical activity are only assessed as changes in physical function measures (e.g., muscle function, grip strength, flexibility, gait speed, postural control) will also be excluded.
To identify relevant studies, the following electronic databases will be searched:
MEDLINE (via PubMed), PsycINFO (via Ovid), Cumulative Index to Nursing and Allied Health Literature (CINAHL) (via EBSCO Host), Cochrane Register of Controlled trials (CENTRAL) (via Cochrane Library), Physical Education Index (via ProQuest), Social Science Citation Index (SSCI) (via Web of Science), Applied Social Sciences Index and Abstracts (ASSIA) (via ProQuest), Sociological Abstracts (via ProQuest), and International Bibliography of the Social Sciences (IBSS) (via ProQuest). Restrictions on English or German language as well as on articles published between 2005 and present will be applied. The search strategy will comprise searching text words in titles and abstracts, where applicable. Search terms related to (1) physical activity, (2) interventions, (3) intervention effects, and (4) older adults will be established by examining previous systematic reviews in the area of interest and discussion between authors. The sensitivity of the search strategy will be tested by examining whether it retrieves several key articles identified in preliminary searches. A sample search strategy for MEDLINE designed in PubMed is shown in Additional file 2.
Searching other resources
The references cited of all articles meeting the inclusion criteria will be screened to capture any relevant publications missed by the electronic searches. To increase the chance of finding relevant articles published in German language not included in the electronic databases, the German language journal Prävention und Gesundheitsförderung (Springer Medizin; volume 1, issue 1, January 2006—volume 10, issue 2, May 2015) will be manually searched.
An EndNote (ENDNOTE X7.1, Thomson Reuters) database will be created to store all citations retrieved by the nine electronic literature databases. Using EndNote’s auto-deduplication function, duplicate citations will be removed. Since auto-deduplication is thought to be only partially successful , the remaining duplicates will be identified by hand-searching techniques. To do this, references will be alphabetically ordered according to the first authors’ names and thereafter according to their titles.
First stage screening
After removing duplicates, first, all remaining titles and abstracts will initially be screened by two reviewers independently. References will be designated as either “not eligible” or “potentially eligible". To differentiate between not and potentially eligible, the following criteria regarding study characteristics, study participants, and interventions will be applied:
Study characteristics: “Potentially eligible” references have to be studies published as an electronic journal article between 2005 and present, and written in English or German language.
Study participants: To be “potentially eligible", the title or abstract must clearly state that the study population comprises older adults or people aged 50 years and over, respectively. Since there is no common definition of “older adults” in the literature, non-specific descriptions, such as “middle aged and older adults", will also be accepted at this stage of screening. References whose titles or abstracts clearly state that the study population is restricted with regard to actual physical activity behavior, functional status, medical conditions, or weight status will be deemed “not eligible".
Interventions: To be “potentially eligible", the title or abstract must be clear that the study reports the effects of an intervention on physical activity behavior. Changes in physical function measures or psychological outcomes only will not be accepted.
Second, both reviewers will compare their decisions and discuss all references generating a disagreement. If necessary, a third reviewer will be consulted. Before consensus will be achieved, inter-rater reliability between the two reviewers will be assessed using a Cohen’s kappa statistic .
Second stage screening
Full texts of potentially eligible references will be retrieved and assessed for final inclusion by one reviewer with a random sample checked by a second reviewer. Following PRISMA guidelines , a flow diagram will be created to illustrate the study selection process, with explanations provided for those studies excluded in the second stage screening process.
Data extraction and management
Data extraction will be conducted by one reviewer and checked by a second reviewer using a pre-designed and pilot-tested data extraction form. It is anticipated that many studies considered social factors described by PROGRESS-Plus only for the description of baseline characteristics of participants. Therefore, a two-stage approach for data extraction will be applied. The following information will be extracted from all included studies (stage one):
Bibliographic details (first author, year of study, publication language, country of study)
Study design and study aim(s)
Eligible participants (inclusion and exclusion criteria)
Intervention details (intervention aim(s), level of intervention and setting, intervention content, control/comparison, intervention delivery, intervention duration, follow-up duration)
Physical activity outcome, outcome measurement, and time points of measurements
Number of participants and PROGRESS-Plus characteristics reported at baseline
Intervention effects on physical activity
Whether study considered PROGRESS-Plus dimensions for measuring intervention effects on physical activity outcome
For studies which examined differential intervention effects by PROGRESS-Plus characteristics (i.e., analyzing subgroup intervention effects or interaction effects by PROGRESS-Plus characteristics), an expanded data collection form will be applied (stage 2). This will include more detailed information on study methods (e.g., method of recruitment of participants, existence of study protocol), intervention characteristics (e.g., theoretical underpinning), and study results (e.g., number and reason for and sociodemographic or socioeconomic differences of withdrawals and dropouts) as well as on the statistical methods used for examining differential intervention effects. Furthermore, information on the ways in which inequalities are expressed (absolute versus relative terms) will be extracted.
Risk of bias assessment of included studies
Quality appraisal of all included studies which examined differential intervention effects by PROGRESS-Plus characteristics will be performed by two reviewers independently. Any disagreements will be resolved through discussion and, if necessary, a third reviewer will be consulted. Quality will be assessed using the Effective Public Health Practice Project (EPHPP) “Quality Assessment Tool for Quantitative Studies” . The EPHPP tool is recommended by the Cochrane Public Health Group as it has been shown to be applicable across a variety of intervention study designs . The tool covers the following domains: (A) selection bias, (B) study design, (C) confounders, (D) blinding, (E) data collection method, and (F) withdrawals and dropouts. Intervention integrity and analysis methods are also appraised.
This systematic review will use a very broad search strategy to capture the entire evidence base on the effects of universal interventions on social inequalities in physical activity among older adults. It is anticipated that this strategy will result in a diverse range of research methods (e.g., regarding study design, intervention characteristics, setting, participant characteristics, outcome measures). Hence, using meta-analysis to integrate and summarize the included studies is unlikely to be appropriate. Instead, a narrative synthesis of results will be conducted, including tables and figures of information relevant for the primary objectives of the review.
To assess the extent to which studies considered effects of interventions on social inequalities, two levels of analysis will be applied: At level 1, we will present data on whether the studies considered various dimensions of social inequalities described by PROGRESS-Plus for the description of baseline characteristics of study participants. At level 2, we will describe whether the studies considered PROGRESS-Plus dimensions for measuring intervention effects and which methods they used (e.g., consideration as confounders by adjusting in multivariate analyses, as effect modifiers in stratified analyses or using interaction terms in multivariate analyses). If feasible, studies which examined differential intervention effects by PROGRESS-Plus characteristics will be synthesized using harvest plots . In addition, the ways in which inequalities are expressed, that is, absolute versus relative inequalities, will be examined, since the decision about whether to measure inequalities in relative or absolute terms may influence their interpretation .