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Predictors of Perceived Social Support for Patients with Dementia: A Mixed-Methods Study

Authors Yang S, Zhang Y, Xie S, Chen Y, Jiang D, Luo Y, Zhao Q, Yang B

Received 11 February 2020

Accepted for publication 11 April 2020

Published 30 April 2020 Volume 2020:15 Pages 595—607


Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Prof. Dr. Zhi-Ying Wu

Siyuan Yang,1 Yunmei Zhang,2 Shiqi Xie,2 Yanhan Chen,2 Dengbi Jiang,3 Yetao Luo,4 Qinghua Zhao,1 Bing Yang2

1Nursing Department, The First Affiliated Hospital of Chongqing Medical University, Chongqing, Yuzhong District, People’s Republic of China; 2School of Nursing, Chongqing Medical University, Chongqing, Yuzhong District, People’s Republic of China; 3Community Health Center of Daxigou, Chongqing, Yuzhong District, People’s Republic of China; 4Department of Biostatistics, School of Public Health and Management, Chongqing Medical University, Chongqing, Yuzhong District, People’s Republic of China

Correspondence: Bing Yang; Qinghua Zhao Email;

Purpose: Perceived social support (PSS) is closely linked to health outcomes in dementia patients. However, its continuous benefits are unclear. This mixed-methods study examined the impact of social support perceptions and differentiation among patients and carers during disease progression.
Patients and Methods: Persons with dementia (PWDs), family caregivers, and community family physicians were recruited from nine community health centers. Semi-structured interviews conducted with 12 PWDs (7 PWDs in mild dementia and 5 in moderate dementia), 12 family caregivers, and 6 community family physicians and conventional content analysis were used to explore social support perspectives at different dementia stages. A total of 470 PWDs were divided into mild (n=224), moderate (n=190), and severe (n=56) groups. Demographic, physical, and psychological factors related to PSS were examined by the group using multiple regression analysis. The group-based characteristics were entered into three prediction models.
Results: In the qualitative study, three themes of social support were identified: two viewpoints refer to social support; different needs and preferences in each stage; non-personalized support services. Quantitatively, the mild group scored lowest in perceived social support, while the severe group scored highest (χ2=64.70, P< 0.001). The mild group PSS was predicted by depression (β=− 0.07, P=0.04), cognitive capacity (β=− 0.18, P< 0.001), and instrumental ability (β=− 0.78, P< 0.001), which differed from the moderate and severe groups.
Conclusion: This study provided comprehensive insight into PSS from PWDs’ perspective at different stages of the disease. Results indicated the need for a stratified care approach and direction for further research on intervention.

Keywords: dementia, illness stages, perceived social support, psychosocial status


Worldwide, over 47 million people currently living with dementia, 96% of whom live at home.1 Notably, China ranks first in the number of patients with dementia (PWDs), accounting for 40% in the Asia-Pacific region and 25% globally.2 PWDs are affected by irreversible and progressive cognitive deterioration, which not only affects their ability to perform daily activities, causes distress, and increases financial burdens, but also places a substantial demand on the social support system.3 In 2017, the World Health Organization established social support as a focal item in its Global Action Plan as a public-health response to dementia and further appealed that PWDs receive better benefits.4 Recent studies have also demonstrated that adequate social support is strongly associated with both psychosocial and general wellbeing among dementia patients.5,6 However, few have directly investigated whether effective social support interventions are applied in China.

Several studies have concluded that social support can be subdivided into two main components: structural support and functional support (also referred to as perceived support).7,8 Perceived social support is most reliably associated with psychosocial and cognitive function. In this context, PWDs typically living with decreased psychosocial status, which leads to apathy, depression, and anxiety.911 The perceived social support framework further outlines the characteristics of patient health needs according to four dimensions—information, esteem, social companionship, and instrumental support12,13—all of which can help patients better cope with stress and the impact of the disease’s physiological processes.14 Based on research by Cohen and Wills,12 the Interpersonal Support Evaluation List (ISEL) is a useful measure of perceived social support corresponding to the four domains of patient health needs and identifies unmet needs among people with chronic diseases.1517 The ISEL successfully compared levels of perceived social support among people with and without dementia in the United States.18 Despite an increasing body of research evaluating social support to provide more effective PWDS interventions,19,20 there is limited awareness of this issue in Chinese society.21 Therefore, we proposed that the ISEL would aid Chinese health providers, allowing them to more efficiently allocate resources among PWDs.

Previous research has shown that western Chinese care providers often do not implement the types and amounts of support required by PWDs,22 regardless of stage and type.23 Unfortunately, elderly persons with chronic diseases are often provided with standardized support systems, which may not be properly tailored to their specific conditions.24 Further, few studies on home-based social support have focused on dementia patients. This poses an important question: does the “one-size-fits-all” approach meet the needs of PWDs and their family members throughout the disease duration? Previous studies have indicated that patients’ perceived social support changes as their diseases progress.25,26 Consequently, several predictors may also lead to different perceptions, including age,27 income,28 changing healthcare climates, negative effects,29 patient service preferences.30 While many predictors have thus been reported, most data were retrieved through clinician and caregiver measurements rather than patient self-reporting. Notably, previous studies have shown that PWDs, including those in the late stages of dementia (MMSE score≥4), can share and exchange ideas, needs, and preferences in meaningful ways and respond to questionnaire investigations,31 providing interaction more likely to improve distress. Regardless, the “one-size-fits-all” approach does not address the specific needs of dementia patients. We do not currently know how perceived social support differs throughout the dementia stages or what predictors are associated with specific areas of patient concern.

The perceptions and predictors of social support are also influenced by PWD’s and family’s culture, health care systems, and insurance.32 For example, dementia is not included in the government-subsidized community health service (CHS) package (eg, hypertension and diabetes), and currently, there is few public health care program specifically for dementia in China.33 For dementia family, extra resources are still belonging to paid services. Moreover, lack of professionals to engage in dementia-specific caring (eg, occupational therapist) is a major barrier to achieve dementia management in CHS in China.34 This study conducted both qualitative and quantitative analyses to examine stage-related differences in perceived social support among dementia patients by testing two hypotheses: (1) there are stage-related differences in perceived social support among PWDs’ perspectives; and (2) there are stage-related predictors of perceived social support among PWDs.

To the best of our knowledge, this study is the first analysis of stage-related differences in perceived social support among dementia patients in China. We, therefore, expected that qualitative interviews were performed to help identify whether any differences, based on stage, exist among PWDs in relation to PSS and what reasons do PWDs experiences of differentiated PSS. Further, a quantitative study was conducted to determine can these predictors explained such stage-related differences in PSS.

Materials and Methods


We conducted qualitative and quantitative research among PWDs, their family carers, and community family physicians from nine districts in Chongqing City. Family carers were contacted first by official accounts on WeChat, posters, mailings, and word of mouth to explain the project and determine interest, and participants were recruited between December 2017 and June 2018. Participants were categorized by phases: (1) acquiring research permission from participating institutions (2) conducting semi-structured interviews with PWDs at different stages of the disease (12 total), their family carers (12 total), and 6 community family physicians that collected data on social support perspectives and any influencing factors; and (3) distributing questionnaires to 470 PWDs (see the Participant Flow Chart in Figure 1) to determine stage-based (mild, moderate, and severe) differences and predictors. This study was initially approved by the Ethics Committee of the First Affiliated Hospital of Chongqing Medical University (Approved No. 2018–084), which is following the Declaration of Helsinki, and registered with the Chinese Clinical Trial Registry (No. ChiCTR1800019678). All community nurses (n=12), community family physicians (n=5), and research team members (n=8) were trained and familiarized with the study protocol and measurements prior to recruitment, questionnaire distribution, data collection, and population screening. Those researchers participated in assessments and received 2-week related-training by the psychiatrist, occupational therapist, and geriatric nurse who staffed in a hospital. The study analysis was only conducted by the program statistician (sixth author), who did not participate in such data collection and population screening.

Figure 1 Flow chart of participants. Abbreviations: MMSE, Mini-Mental State Examination; ISEL-12, Interpersonal Support Evaluation List-12.


Inclusion criteria included: (1) age 65 or older; (2) dementia diagnosis by a neurologist based on the International Classification of Disease, Tenth Revision (ICD-10) or a Mini-Mental State Examination (MMSE) score≤24; (3) spoke Mandarin (Sichuan dialect) as their primary language; (4) were community-dwelling (day-care center or at home); (5) not bedridden; (6) had family caregiver, or had a contact at least 4 days or 7 hours per week. Family carers and community family physicians were included if they had at least one-year experience for caring PWDs. All participants were informed about the voluntary nature of this study and that they could withdraw at any time; each participant provided written informed consent to participate.

Exclusion criteria included: (1) an MMSE score<7;35 (2) hearing was inadequate for conversation; (3) vision inadequate to read text written in 22 pt. font; (4) unable to complete the ISEL scale. Caregivers who were inability to understand Mandarin (Sichuan dialect) or had mental health problems and those who were not willing to participate were also excluded from this study.


For the qualitative component, participants were enrolled through purposive sampling at the Daxigou Community Health Center and the Shangqingsi Community Health Center (PWDs’ MMSE score range: 12–22). A total of 33 participants were contacted by telephone and the study was explained in detail by the first author. Thirty participants agreed to take part in the interviews (Table 1). Two PWDs (MMSE=13, MMSE=16) refused to complete the interview, citing personal reasons; one interview was paused when the PWDs (MMSE=20) became emotionally unstable.

Table 1 Participant Characteristics in Semi-Structure Interview (n =30)

For the quantitative component, a total of 474 PWDs were recruited through convenience sampling from nine community health centers (Daxigou, Shangqingsi, Xiejiawan, Shapingba, Lianglukou, Shiqiaopu, Huaxinjie, Lianglu, and Longshan; Figure 1). A total of 772 PWDs were contacted by the community health workers to screen for eligibility; 545 were eligible and 227 did not meet eligibility criteria because of: age<65 (n=26), MMSE score>24 (n=79), MMSE score<7 (n=37), bedridden (n=15), caregiver not available (n=18), hearing inadequate for conversation (n=16), impaired vision prevented reading 22 pt. typeface (n=11), and did not provide informed consent (n=25). The final analysis included 470 participants; 71 PWDs were excluded for: unable to complete the ISEL (n=21), missing data (n=31), or withdrew without providing a reason (n=19).

Assessment Instruments

Qualitative Data

The semi-structured interview schedule comprised open-ended questions designed to elicit participants’ perceptions, experiences, and views of social support. Patients were asked: what supports have you received so far (how do you feel), what you experience in daily life, and what else do you need. Family caregivers and community family physicians were asked: what is social support, what supports do you provide for PWDs; what difficulties do you have taking care of her/him (how do you feel); and what things influence social support. Interviews were independently conducted and recorded in the individual homes or daycare centers and lasted between 15 and 46 minutes. All recordings were transcribed for analysis. Field-notes were made to record observations and reflections of the interviews. The interview was paused and comfort provided when the interviewee became emotionally unstable.

Quantitative Data

Information was collected based on Cohen’s social support theory.12 In accordance with previous studies and qualitative findings,36 PSS related factors, such as daily activities, cognitive function, psychosocial status, and demographics (ie, physical health status and caregiver type), were collected to explore stage-based differences in perceived social support and any predictive variables. Outcome measures included six questionnaires with well-established validity and reliability, as described in Table 2. The Neuropsychiatric Inventory (NPI; including nighttime behaviors, irritability, apathy, depression, and motor disturbance), Mini-Mental State Examination (MMSE), Interpersonal Support Evaluation List-12 (ISEL-12), Activities of Daily Living (ADL), and Functional Assessment Questionnaire (FAQ) were administered to all PWDs. All questionnaire items were completed through face-to-face interviews, which conducted by trained research staff. Demographic information was collected from an information questionnaire and community healthcare center records. All questionnaires were self-report except the NPI. We adapted the questionnaires to improve data collection efficiency, such as increasing the font size, using graphics instead of text, using dichotomous answers (yes/no), and providing scenario simulation.

Table 2 Study Measures, Descriptions, and Reliability


All qualitative data were used as a conventional approach to content analysis. Information of all samples (PWDs and carers) was summarized and transcribed using Microsoft Word.37 The iterative analysis process included: (1) First and second authors jointly read each transcript. (2) Highlighted the words or phrases which described the meaning and feelings of social support. (3) These keywords or phrases were formed into codes. (4) Co-researchers checked all the data in the specific codes. (5) Added new codes when researchers encountered data that did not fit into existing code. Information saturation was achieved when no new themes emerged. (6) Discussed codes with co-researchers and used to supplement and refine the coding scheme. (7) Classified codes and grouped into descriptive categories.

Quantitative data were analyzed with IBM SPSS Statistics, version 23.0 (IBM Corporation, Armonk, NY, USA). Patients were grouped into three categories based on their CDR scores (ie, mild: CDR 1, moderate: CDR 2, and severe: CDR 3 and MMSE≥7). The Pearson’s χ2 test was then used to compare stage-based categorical variables; analysis of variance and Kruskal–Wallis H-tests were performed to compare the mean values of the continuous variables. Bonferroni post hoc adjustments were used. Statistical significance was set at P < 0.05 for all analyses.

Multiple linear regression analyses were then used to determine the predictors of perceived social support for each group. All variables were forced into the model for simultaneous control, including age, sex, education, socioeconomic status, physical health status, caregiver type, and the PSS, ADL, FAQ, NPI (nighttime behaviors, irritability, apathy, depression, and motor disturbance), and MMSE scores. The multivariate linear regression analysis model fit was tested by model-residual and normal-probability graphs. Weighted multiple regression analysis was used in the presence of heteroscedasticity.


Qualitative Findings

Two Viewpoints in Social Support

Both PWDs and carers (Table 1) described social support as receiving assistance to improve living conditions. However, an interpretation of social support revealed two separate aspects of their concern. A mild patient [P02 (MMSE score=20)] said, “ … make easier [life] but now, I am afraid of going out … I want her [wife] to go out with me … ”; a moderate patient [P03 (MMSE score=12)] said, “ … she [wife] is here … I feel safety ….”; a community family physician [CC04] stated, “I think, it means the amount of supports would be available if it was need[ed] … ”; and a family caregiver [FC02] said, “I almost spend all my time … tired … [sigh] … I have to take charge of all things … eating, drinking, and excretion” [patient at severe stage]. “The more time and efforts you spend on the patient, the better life he (she) gets”, another family caregiver [FC04] stated.

As indicated, patients and caregivers all acknowledged the positive impact of social support. However, PWDs were more focused on the “functional features” of social support (eg, they can perceive assistance and accompany which provided from caregivers), while carers tended to focus on the “structural features” (eg, time-consuming care and type of social support).

Different Needs and Preferences in Each Stage

Lower levels of respect and restricted social activities were described in mild-stage patients. As shared by a mild patient [P07 (MMSE=19)], “ … shame on me [husband], he sometimes likes to talk about it with others [dementia].” Another mild patient [P04 (MMSE=18)] stated,

… I’m just older and slower … actually … being able to care for myself … they [husband and sons] insist [on] me staying at home and restrict other independent behaviors for safety … it’s not as bad as what they said [frown] … they had me as an imbecile.

“perceived Independent and respect” described their perceptions about what reflecting great experiences for social support. Most mild-group patients reported negative emotion, “ … sometimes I feel boring … have been sitting at day-care center watching television … no talks to others … what’s happening to me [frown]?” as shared by another patient [P05 (MMSE score=21)]. “emotional input” described their perceptions reflecting what support is required for them.

For advanced PWDs, more stable emotional supports were demonstrated. A higher need for “accompany and assistance” was reflected in moderate patients [P01 (MMSE=14)], “ … okay … she [wife] is here [at home] ….” That perspective of acceptance was shared by another patient [P02 (MMSE=13)]. Patients with moderate dementia worried about uncontrollable behavior, which was reported as the most stressful matter. A moderate patient [P04 (MMSE=15)] stated, “I always awoke [at midnight] … [gloomy], she [daughter] always consoled me ….”

Non-Personalized Support Services

Although caregivers lived with greater mental and physical pressure when patients were sick, they were still willing to maintain their roles, especially family members. In that case, most of them reported that the actual needs of PWDs were “hardly understanding”. An unpaid caregiver whose husband had severe dementia [FC02] stated,

Although my burden is pretty heavy [sigh], as his wife, it’s my obligation to care for him … I feel so tired … it’s hardly [the type of] communications as it was previously … I can guess his emotion if he gives me some words or expressions.

Another unpaid carer [FC05] reported,

My mom [with mild dementia] became more and more reluctant to talk when she knew her situation … suddenly showed to be unhappy or upsetting … I don’t know, what good coping strategies can take me to escape from this problem. …

Compared to the unpaid caregiver, less understanding of PWDs was reported by paid caregivers. One paid caregiver [FC10] said, “ … It’s hard for me … like understanding their [with severe dementia] emotional change.” For paid caregivers and family physician, “usually care” described their perceptions of supports in caring. Patient perspectives were rarely considered when making decisions during routine community-conducted home visits. One community family physician [CC03] stated,

… [we] provide more concerns with non-differential management of chronic diseases for patients … and indeed, it is hard to provide person-centered care … cannot fully understand everyone’s needs, especially PWDs ….

Another community family physician [CC04] said,

… we provide visits services for them [PWDs], which focused on their basic needs and symptoms management … … no, no occupational therapy and counseling … like other chronic disease management … the regulation visits [service times] are twice a week.

Quantitative Findings

Overall, the refusal/non-response rate was 39.1%. The 470 PWDs enrolled in the quantitative study had a mean age of 78.3 years (SD 7.3). The mild group included 224 participants (47.7%); 190 (40.4%) were in the moderate-group; and 56 (11.9%) were in the severe group. Demographic data are presented in Table 3. There were no major between-group differences in sex, age, education, socioeconomic status, physical health status, or caregiver type.

Table 3 Demographic Characteristics (n = 470)

Significant within-group ISEL-12 score differences are shown in Figure 2. Notably, ISEL-12 scores (mild dementia group= (21.25±3.13), moderate dementia group= (22.49±5.65), and severe dementia group= (26.98±3.08)) increased with disease severity (χ2=183.16, P<0.001). There were also significant within-group differences for the MMSE (range: 7–24), ADL, FAQ, and NPI (sleep, irritability, depression, and behavior) scores, whereas no significant difference emerged for apathy. Based on this finding, we expect that these different factors represent distinct stages of PSS perception.

Figure 2 Scores of mean and SD in ISEL-12, ADL, FAQ, NPI, and MMSE among the AD with mild, moderate, and severe stage. Notes: ***Significant difference among the three groups (P≤0.001). Abbreviations: ISEL-12, Interpersonal Support Evaluation List-12; ADL, activities of daily life (the 100 points were converted to 20 points); FAQ, Functional Assessment Questionnaire; NPI, Neuropsychological Inventory (nighttime behaviors, irritability, apathy, depression, and motor disturbance); MMSE, Mini-Mental State Examination.

The multiple regression model (Table 4) for the mild group explained 79.0% of the total variance of ISEL-12 scores, which was predicted by depression, FAQ, MMSE scores, and age. Better cognitive function, more limited instrumental daily activities, and depression were associated with lower PSS. Compared with advanced dementia patients, those with better cognitive function were more aware of the related psychosocial effects. In the moderate group, predictors included education, behavior problems, ADL, FAQ, and MMSE scores, which explained 75.1% of the variance in the ISEL-12 scores. Lower PSS was predicted by lower education, high levels of behavioral problems, daily activities, and better cognitive capacity. In the severe group, 64.4% of the total variance in the ISEL-12 scores was explained by caregiver type and ADL. Lower PSS was predicted by paid caregivers and better basic daily living abilities. It means that in advanced dementia, awareness deficits tend to be a protective factor of PWDs with reduced cognitive capacity, which might contribute to their improved subjective experience.

Table 4 Multiple Regression Results for the Perceived Social Support Scores of Dementia by Stage Groups (n = 470)


This was the first study to explore how PSS differed among PWDs at different disease stages in China and to identify the factors associated with these differences. Qualitative data analyses suggested that a divergent interpretation of social support and limited psychosocial support mainly contributed to low PSS reported by patients with mild dementia. There were two main quantitative findings: (1) patients with mild dementia had worse PSS than patients at more advanced stages; and (2) PSS predictors differed by group (mild, moderate, and severe). These findings validated our two hypotheses, thus adding to the social support literature by verifying different levels of perceived social support at different stages of the disease.25

As noted, BPSD (ie, agitation, depression, apathy, aggression, sleep problems, wandering, and a variety of socially inappropriate behaviors) episodically fluctuate throughout the dementia stages.38 This contributes to perceived social support impairment.9 This study found certain BPSD factors (ie, depression and motor disturbance) were significantly associated with relatively lower PSS in mild and moderate patients. These results may explain previous findings reporting more episodes of BPSD in mild and moderate patients than advanced patients.39 Fluctuating psychosocial symptoms may be caused by impaired left-hemisphere emotional regulators,40 while in advanced-stage patients, this may weaken functioning while suppressing negative emotions, thus making individuals more inclined toward positive effects.41,42 The qualitative results showed that carers did not pay attention to or deal with patients’ negative emotions; this may result in lower perceived social support, which was reported by mild dementia patients more often than by those in severe stages.

Interestingly, better cognitive function was another predictor of worse PSS in mild-dementia patients. The narrative descriptions obtained from mild-group patients and their carers provided additional insight into the mechanism underlying lower PSS among mild dementia patients. Compared with advanced dementia patients, those with better cognitive function were more aware of the related psychosocial effects. Most believed that dementia threatened the meaning of life, their individual identities, and their overall wellbeing. Consequently, these patients tended to avoid dementia-related information (eg, showing impatience or shame when discussing disease-related topics). This finding was consistent with a previous study by Cheston et al, in which mild dementia patients had poor recall of dementia-related information when it referred to them as opposed to other persons.43 Traditional Chinese values emphasize moral excellence and self-cultivation of harmony within the self, family, and society, however, dementia symptoms such as BPSD have broken this harmony. Most families of people with dementia refused to disclose the condition to avoid stigma and it marked respect lacking in society.21 Therefore, psychosocial processes related to threat awareness may result in lower PSS levels in those with mild dementia. Conversely, in patients with advanced dementia, awareness of deficits tends to decline with reduced cognitive capacity, which might contribute to their improved subjective assessment.35

Notably, we found that PWDs and their carers had different perspectives on social support. For instance, mild dementia patients were more positive about their own social abilities than were their family members. However, we were unable to determine whether these differences result from patient underreporting and/or carer overreporting, but as a patient said,

… I’m just older and slower … actually … being able to care for myself … they [husband and sons] insist [on] me staying at home and restrict other independent behaviors for safety ….

Further, PWDs tended to concentrate on their inner degree of social support in terms of understanding it, while carers typically paid attention to the frequency and size of the support, believing, “The more time and efforts you spend on the patient, the better life he (she) gets.” Conflicting perspectives may accentuate patients’ negative emotions and make them feel disrespected. These contradictions may also reflect the important roles of negative emotions and perceptive gaps in social support, thus explaining the overall lower perceived social support in mild dementia patients.44

In contrast to patients with mild-to-moderate dementia, we found that the “pleasant or gentle response” was most prevalent in the severe group when they were with family caregivers. For example, moderate-stage participants demonstrated a weaker desire for interaction, or “relationship numbness,” as general apathy or reluctance developed. When family carers communicated with recipients through vocalizations, bodily contact, and gestures, severe patients frowned less frequently and showed more relaxed expressions compared to those in less severe stages. Our quantitative results indicated that individuals with severe dementia cared for by relatives had better PSS; severe patients were more dependent on their carers because of declines in linguistic competence and daily living activity; and intensive interaction and sense of security occurred more between family members, especially in the context of Chinese culture.45 This is based on the previous shared experiences of communication, including eye gaze, emotional expression, and movements.46 However, patients’ habitual nonverbal attempts might be typically ignored47 or judged incomprehensible48 by paid carers, who formed relationships with PWDs who already had significant linguistic barriers by the time they met.49 Most caregivers lack training and education on management of dementia in China, such as cognitive exercises and rehabilitation, only provide basic care on eating, dressing, and bathing. Additionally, caregiver populations were lacking employment access systems, resulting in employee caregivers usually as a nanny.50 Therefore, support from a close family member related to all-day basic living care and better emotional sharing, which may result in higher levels of perceived social support from patients in later stages.

Strengths and Limitations

This study had several strengths, including (1) its examination of a large Chinese community-based cohort, (2) a mixed-methods approach to assess perceived social support across three dementia stages, (3) an original perspective in differentiating perceived social support in terms of dementia progression, and (4) a broad analytical approach to examining lower perceptions of social support among patients with mild dementia. The main criticism that may be levelled at this study is that it included severe dementia patients as participants. In the qualitative study, although severe PWDs were not interviewed directly, we obtained their social support status through limited verbal feedback, observation of expressions and behaviors, and communication with their caregivers; we enrolled PWDs with MMSE≥7 in the quantitative study, most of whom had the ability to complete questionnaires.51 In addition, we did not intensively investigate participant structural support; instead, we assumed that the “size” of their social network would be similar to that of older persons under the Chinese unitary community health care model. Finally, we only examined data from western China. Therefore, our findings may have limited generalizability.


In China, mild dementia patients experienced the lowest perceived social support. Perceptions and predictors differed according to the relative salience of perceived social support in each stage. Further, the predictors of social support can become “moving targets,” with different symptoms appearing at different stages of the disease. This reinforces the importance of performing specific evaluations and interventions that are tailored to patient needs. This study provides guidance for stage-specific clinical practices and those looking to develop community-based, long-term care systems for dementia patients.

Data Sharing Statement

Individual participant data that underlie the results reported in this article will be shared, after deidentification (text, tables, and figures). Data are available for beginning 9 months and ending 36 months following article publication. Proposals should be directed to To gain access, data requestors will need to an agreement. Additionally, no further data will be shared besides what is included in the manuscript.


This work was supported by the Chongqing Science and Technology Commission (Grant nos cstc2017shmsA10001 and cstc2018jscx-mszdX0013). The authors thank the patients and their caregivers. We are also grateful to doctors and nurses in the First Affiliated Hospital of Chongqing Medical University and community health workers for participating in this study.


The authors report no conflicts of interest in this work.


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