This report presents results based on the longitudinal findings from Waves One and Two of the Life Opportunities Survey. A second report, focussing on the cross-sectional findings from the second wave of the survey, as well as additional longitudinal analyses, will be published in 2013.
The Life Opportunities Survey (LOS) is a large-scale longitudinal survey of disability in Great Britain and it is the first major national social survey which explores disability in terms of the barriers to participation that people experience. Prior to the development of the LOS, the last major survey on disability conducted in Great Britain had been the Family Resources Survey disability follow-up in 1996/97, and before this were the Office of Population Censuses and Surveys (OPCS) national surveys of disability carried out during 1985-88. In 2005, the Department for Work and Pensions (DWP) carried out a feasibility study which recommended a new survey dedicated to meet the evidence needs of the policy for disabled people in Great Britain. Subsequently, the Office for Disability Issues (ODI) (part of the DWP) commissioned ONS to develop the LOS.
The survey is wholly funded by the DWP and is carried out by the Office for National Statistics (ONS). Each wave of the survey spans two years and respondents are followed up approximately one year after their initial interview. Wave One of the LOS took place between June 2009 and March 2011; Wave Two began in June 2010 and finished in March 2012.
According to the social model, disability is viewed as the disadvantage, or restriction of activity and participation, caused by aspects of society which take little or no account of the needs of people with impairment. Therefore, in line with the social model, the LOS assesses the level of participation of people with impairment and the barriers to participation they face.
Impairments relate to the loss of physiological and psychological functions of the body such as loss of sight, hearing, mobility or learning capacity and should be distinguished from medical conditions or loss of bodily structure. For example, glaucoma is a medical condition whereas loss of vision is the impairment it causes. Activity limitations are restrictions an individual may have in executing physical or mental tasks or actions as a result of their impairment, for example, being unable to read newsprint at arm’s length without glasses or other aids and adaptations.
The LOS collects self-reported data on impairment, this is dependent upon the respondent’s perception of the limitations and severity of the impairment.
In this report, an adult is defined as having an impairment if they indicated that:
they experience either moderate, severe or complete difficulty within at least one area of physical or mental functioning, and
certain activities are limited in any way as a result. ‘Activities’ refer to different areas of physical or mental functioning, such as walking, climbing stairs or reading a newspaper.
The LOS collects information about all impairments that a respondent may have (it is possible for a respondent to report more than one impairment) and respondents are asked to self-classify their impairment according to a list of 14 impairment types (sight, hearing, speaking, mobility, dexterity, long-term pain, chronic condition, breathing, learning, intellectual, behavioural, memory, mental, and ‘other’). At Waves One and Two of the survey respondents were not asked to specify the underlying condition for each impairment type however respondents who reported a particular impairment were asked the level and frequency of the limitation caused by the impairment. Questions about long-term health conditions were also included.
This method of classifying impairment status is compatible with the International Classification of Functioning, Disability and Health (ICF) developed by the World Health Organisation (WHO).
The survey also collects information on:
participation in different areas of life
the barriers that people face to participating in these areas of life
how levels of participation and barriers to participation change over time
Examples of barriers include: discrimination, the attitudes of other people, inaccessible buildings, public transport and information, limited income, not having anyone to meet or speak to, as well as lack of support, equipment and adjustments.
Respondents are asked questions on a broad range of topics including employment, education and training, transport, leisure, social and cultural activities, the accessibility of buildings and use of public services. They are also asked questions about social care, experiences of discrimination and crime and the financial situation of the household.
The LOS asks questions about people’s experience of barriers in the following eight life areas:
education and training
economic life (the household’s ability to make ends meet)
accessibility in the home
accessibility outside the home
Further information on the development of the survey, including details on the consultation with a reference group of disabled people and qualitative testing of the survey, can be found in the Wave One Interim Report.
The data analysed for this report came from respondents who were interviewed in both Wave One and Wave Two of the LOS. This report focuses only on the longitudinal aspect of the data; Part II of the report (due to be published in 2013) will focus on cross-sectional findings, that is, results for Wave Two (alongside comparisons with Wave One cross-sectional findings), as well as further longitudinal findings.
The following section of the report contains a brief summary of how respondents are followed up from Wave One to Wave Two, and how they are classified into groups for the purpose of longitudinal analysis. The analyses presented in subsequent chapters are also broadly outlined in this section.
Each respondent’s impairment status at Wave One was used to assign them to one of three different groups which determined how they were followed up at Wave Two:
This group included all adults who reported at least one impairment at Wave One (29 per cent). These adults, as well as all adult members of their households, were interviewed in person at Wave Two.
Of the 71 per cent of adults who did not report having an impairment at Wave One a subset was selected to form a ‘control’ group. The adults in this group were chosen to provide a comparison group that is similar to the adults with at least one impairment on several key characteristics associated with impairment – sex, age, region of residence, and the urban/rural classification of residence. The size of the control group was designed to be half that of the group of adults with at least one impairment, that is for the Wave Two sample there were two adults with impairment for every one person in the control group. All of the adults in the control group, as well as all adult members of their households, were interviewed in person at Wave Two. Analysis of results from this group will be included in the LOS Wave Two Report, Part II
For more information on the composition of the three follow-up groups, see the Wave Two Technical Report, to be published in 2013. Alternatively, see the Wave Two Interim Technical Report (2.26 Mb Pdf) .
Figure 1 shows how adults have been classified for the longitudinal analysis. The classification takes into account impairment status at both Wave One and Wave Two. Figure 1 also illustrates how adults who did not report any impairment at either Wave One or Wave Two flow through the survey.
The following three groups are featured in the longitudinal analyses of this report:
Adults with at least one impairment at both waves.
Adults with no impairment at Wave One but reported at least one impairment at Wave Two.
Adults with at least one impairment at Wave One, but did not report any impairment at Wave Two.
The main focus of the chapters that follow will be on adults who reported impairments at one or both waves. Chapters 2 to 4 will describe the three groups (adults with impairment at both waves, adults who have offset from impairment, and onset-acquired adults) in turn, focussing on the number, types, and severity of impairments these groups had reported.
These chapters will also give measures of the likelihood of impairment onset and offset (onset and offset rates), across several demographic characteristics. In Chapter 5, changes shown by the three groups across the two waves, in economic activity status, income distribution, and participation restriction across life areas, will be examined. Finally, Chapter 6 will give a summary of the general findings for these three groups.
The data has been weighted to provide estimates for the general population.
Detailed definitions of the terms and categories used in this report are provided in the Glossary at the end of the report. All estimates presented in the tables and charts have been analysed using longitudinal weights so that they have been adjusted for non-response, differential sampling probabilities of selection at Wave One, and loss to follow-up at Wave Two1.
Percentages reported throughout the document have been calculated using population estimates rounded to integers. When calculating percentages, the values of residual categories such as ‘no answer’ or ‘don’t know’ have been excluded from the denominator. Percentages are rounded to zero when there are fewer than three adults contributing to an estimate.
The response rate for LOS Wave Two can be calculated at both household and individual level. The LOS Wave Two achieved a household level response rate of 73 per cent. In this case responding households were those in which information was collected in person or by proxy for all adults. The survey achieved an individual response rate of 73 per cent, among adults who were eligible for a face-to-face interview. The response rate for adults selected to form the control group was slightly higher than for adults with at least one impairment at Wave One (77 per cent compared with 74 per cent respectively).
For longitudinal surveys, the sample is subject to attrition moving from one wave to the next. For the LOS, a subset of the original sample at Wave one were not contactable, did not respond, or refused further participation at Wave two. More information on sample attrition and the household and individual response rates can be found in the Wave Two Technical Report, to be published in 20132.
Unless otherwise stated, changes and differences mentioned in the text have been found to be statistically significant at the 95 per cent confidence level.
LOS is a longitudinal survey that has been designed to follow respondents over time to provide an insight and understanding into the transient nature of impairment. A key component of the survey design is the ability to compare the experience of barriers to participation between people with impairment and those without impairment over time to assess the equality in access in different life areas. The formation, at Wave Two, of a control group from within the respondents who did not have any impairments at Wave One, will allow experiences to be compared between the two groups over time.
Survey design. The LOS uses an unclustered sample designed to produce efficient estimates for the sample size and Great Britain. The unclustered sample allows greater precision to be achieved in LOS outputs because it helps to make the sample more representative of all groups in society.
The size of the Wave One sample was sufficient to accommodate for attrition over time. As a result, at Wave Two, the sample remains of a sufficient size to allow for comparisons and analysis to be conducted among subgroups of the sample.
The LOS is a sample survey and so is subject to weaknesses which also exist for other surveys, including:
Non-sampling error. Estimates from all sample surveys, including those derived from the LOS data, will contain a degree of uncertainty due to non-sampling and sampling error. Non-sampling error generally arises from errors in the collection, measurement and processing of the data. To minimise non-sampling error the LOS questionnaire was administered using computer assisted interviewing (CAI), which ensured that the questionnaire routing was followed correctly during the interview and inconsistencies and potential collection errors were able to be queried, and where appropriate, corrected during the interview. Again, to minimise non-sampling error, as a result of errors arising from data collection, all ONS interviewers received both generic interviewer training and specific LOS training prior to working on the LOS. The LOS Wave One Technical Report provides further information about the data collection and processing of the data.
Sampling error. This relates to the fact that the sample chosen is only one of a large number of samples which could have been chosen. It follows then that any estimate derived from the sample is only one of a large number of estimates which could have been made. For users of survey data, the precision of the estimate is of interest, that is, how much the estimate would vary when different samples are drawn1. In general, the larger the sample size from which the estimate is derived, the more precise, or robust, is the estimate.
Sample size. All tables contain figures based on sample estimates that have been weighted so that they apply to the overall population. This involves the use of a set of adjustment (or grossing) factors that attempt to correct for differential attrition between Wave One and Wave Two. The unweighted sample counts, shown in the tables as ‘sample size=100%’, therefore can help users to judge the robustness of the information (the larger the sample size the more robust the relevant estimate). Note that the unweighted sample counts have been rounded to the nearest 10. All figures in this report have been rounded independently. Therefore, the sum of component items will not necessarily equal the totals shown.
Non-response and missing information. The information from a household which co-operates in the survey may be incomplete. This can be due to one of the following reasons: i) a partial refusal (e.g. to income); ii) because information was collected by proxy, therefore certain questions were omitted from the interview; or iii) a particular item was missed because of a lack of understanding or an error.
Households who did not co-operate at both Wave One and Wave Two are omitted from all analyses. Those who omitted whole sections because they were partial refusals or interviewed by proxy are not included in the analyses of that section. The ‘no answers’ arising from omission of particular items have been excluded from the base numbers shown in the tables and from the bases used when calculating percentages.
Missing answers are excluded from the tables and in some cases this is reflected in the sample bases, i.e. these numbers vary between tables. For this reason, the weighted bases are excluded from tables as they are not recommended as a source for population estimates. Recommended data sources for population estimates for most socio-demographic groups are: ONS mid-year estimates, the Labour Force Survey, or Housing Statistics from the Department for Communities and Local Government.
Survey coverage. The LOS Wave One sample was designed to cover private households in Great Britain. Therefore individuals in care or retirement homes, for example, will not be included. This means that figures relating to the severely disabled and the most elderly individuals may not be representative of the Great Britain population, as many will have moved into homes where they can receive more frequent help.
The survey at Wave Two follows individuals, and their households, and remains a private household survey. This means that any respondents who have moved into institutions (care or retirement homes, prison, etc) between waves one and two were not followed at Wave Two and were recorded as not eligible to participate in the survey.
The LOS Wave Two set sample comprised only of households of individuals who had participated at Wave One and did not include any new households. This approach does not allow the sample to be refreshed to include any new population sub-groups that may have entered the country since the sample was drawn for Wave One. However, any adult or child who had entered a LOS household since the Wave One interview are included as new survey entrants at Wave Two.
Survey bias. Although work has been undertaken to try to ensure that the figures that have been collected are valid and that adjustments are made for attrition, survey bias may still remain. This may be partly due to misreporting of certain data items and sampling error, but also may reflect non-response biases not controlled for in the weighting factors. Efforts are continually being made to minimise these problems, for example through greater reliance on documentary evidence at the interview and maintaining response rates.
Potential under or over reporting of impairment. The LOS collects self-reported impairment data which is dependent upon the respondent’s perception of the limitations and severity of the impairment at the time of the interview. A self-reporting measure of this kind is prone to both over and under reporting as the perception of the existence and effect of impairment is dependent upon each respondent’s own personal opinion on the day they are interviewed.
One consequence of this is that respondent’s perception of the impairment may differ over time causing transitions to be recorded that may or may not be real. For example, the LOS definition of impairment is dependent upon the respondent reporting more than ‘mild’ difficulty. If at Wave One they report ‘moderate’ difficulty they will be classed as having an impairment according to the LOS definition, however if at Wave Two we assume that there has been no change in the impairment and the respondent reports ‘mild’ difficulty, LOS will no longer class them as having an impairment. Using this example, the respondent will be treated as having offset from impairment at Wave Two.
The results from the longitudinal analysis of the LOS will be used to inform a new understanding of the dynamic nature of the disabled population and of the barriers faced by people with impairment. It is important to understand more about the dynamic nature of disability to inform policy development in particular on the support people need during onset of impairment. As well as looking at barriers, future waves of LOS will also collect information on the key enablers to removing barriers. This will inform the development of the approach the Government will take in helping disabled people to fulfil their potential and have the opportunity to play a full role in society.
The LOS Wave Three questionnaire will include questions designed to collect information about onset and offset of impairment. In particular additional questions will be asked to provide understanding of any enablers that may have resulted in the removal of barriers to participation in particular life areas. It is hoped that the information collected by these new questions, at Wave Three, will allow further understanding of survey error, in particular the extent of mis-reporting of changes in experience of participation restriction.
A summary of this report is available in alternative formats such as Large Print, Braille, Audio or Easy Read. The Easy Read and Audio versions are available via the ONS website and Large Print and Braille copies are available from the ONS LOS team. Contact the LOS team by email LOS@ons.gsi.gov.uk or by telephoning +44 (0)1633 455296. The LOS wave two datasets will be made publicly available in 2013, via the UK Data Archive, following publication of Part II of the LOS Wave Two Report subject to DWP's agreement.
Details of the policy governing the release of new data are available by visiting www.statisticsauthority.gov.uk/assessment/code-of-practice/index.html or from the Media Relations Office email: firstname.lastname@example.org