Correlates of spiritual wellbeing in persons living with Parkinson disease
Introduction
Spirituality often is a significant part of an individual’s life. Yet, spirituality and its role in coping with chronic medical conditions has only recently been examined (1). Investigators have documented improved self-management behaviors, or to mental states such as happiness, optimism, and hope, all of which are related to better health outcomes associated with higher levels of spirituality (2). Research suggests that the positive association between spirituality and coping may be due to individuals with high levels of spirituality using more diverse and varied coping techniques to manage illness (3). Conversely, negative spiritual coping techniques (e.g., feeling punished by God) are associated with increased distress, depression, and impairment in quality of life (QOL) possibly resulting in hopelessness and despair (4). Despite this clear relationship between spirituality and coping with illness, little is known about spirituality and Parkinson disease (PD).
Exploratory research in PD and spirituality indicates that many PD patients rely on faith to find a deeper meaning and purpose in their illness. A cross-sectional study with PD patients in a Colorado clinic found that 59% reported using prayer to cope with their illness, and 67% of that patient subset felt prayer led to improvements in disease maintenance (5). Spiritual coping mechanisms, such as surrendering to a higher power, are frequently beneficial in managing symptoms and disease (6). A qualitative study on PD and spirituality noted distinct themes affecting faith and coping, including: dependence on belief and faith, providing purpose and meaning, establishing a connection with God by praying, establishing a connection with other individuals, and feeling a sense of gratitude and hope (7). Spiritual and religious practices may serve as a crucial means of defining and managing PD for these patients.
Spiritual distress is an integral component of palliative care assessments and treatments, necessitating the inclusion of spiritual counselors on palliative care teams. As PD is now an area for palliative care delivery, spiritual distress in both patients and caregivers, as well as the relationship between spirituality and palliative symptoms in PD, need to be better understood to optimize spiritual palliative treatment for PD patients. Goals of the present study are to (I) examine the correlation of patient spiritual distress with mood, caregiver engagement, disease status, and caregiver spirituality, and (II) determine whether spirituality modulates correlation of QOL and other predictors in PD. Results of the study can be used to inform the practice of spiritual counselors engaging with PD patients and caregivers, specifically in palliative care settings.
Methods
This cross-sectional study is based on the baseline data of a larger randomized, controlled trial, described in greater depth in a separate manuscript (8). This study was conducted through three medical institutions with currently operating outpatient palliative care clinics for PD, and institutional ethics review board approval was received for each of the three study sites. Participants were recruited through specialized movement disorders programs, community neurologists, and self-referral from patients. One caregiver was enrolled for each participant, when available, by asking PD patients, “Could you please tell us the one person who helps you the most with your PD outside of clinic?”.
Participants
Participants were eligible if they were fluent in English, over 40 years of age, and met criteria for diagnosis of PD, progressive supranuclear palsy (PSP), corticobasal degeneration (CBD), multiple systems atrophy (MSA), or Lewy body dementia (LBD). Individuals also had to be assessed as high-risk for poor outcomes based on screening with the Palliative Care Needs Assessment Tool (PC-NAT) modified for PD. Participants were excluded based on the following factors: (I) immediate and urgent palliative care needs (these patients were not randomized into the larger trial and were offered appropriate services immediately); (II) unable or unwilling to commit to study procedures; (III) presence of additional chronic medical illnesses which may require palliative services (e.g., metastatic cancer); or (IV) already receiving palliative care and/or hospice services.
Outcome measures
All outcomes reflect baseline measurements only. The primary outcome measure for the study was the Functional Assessment of Chronic Illness Therapy - Spiritual Well-being (FACIT-Sp) (9,10), a 12-item scale with responses scored on a 5-point Likert scale from 0 to 4. The measure has three subscales: the sense of meaning, the feeling of peace, and the role of faith in illness. A summary score of spiritual well-being was calculated, ranging from 0 to 60, with higher scores indicating greater spiritual well-being (9,11).
QOL
Because no QOL measure has been validated for a palliative PD population, several measures were used to assess QOL, including: the Parkinson’s Disease Questionnaire 39 (PDQ-39) (12), the McGill Quality of Life Questionnaire (McGill QOL) (13), the Patient-Reported Outcomes Measurement Information System (PROMIS-29) (14), and the Quality of Life in Alzheimer’s Disease (QOL-AD) (15).
Mood and cognition
The Hospital Anxiety and Depression Scale (HADS) measured self-reported anxiety and depression and has been validated in outpatient settings (16). Cognition was assessed with the Montreal Cognitive Assessment (MoCA), which is commonly used to assess cognitive status in PD populations (17).
Advance care planning
Participant possession of a completed Physician Order for Life Sustaining Treatment (POLST), Medical Orders for Scope of Treatment (MOST), or other advance directive (AD) was measured at a nominal (‘yes’ vs. ‘no’) level.
Physical symptoms
Physical symptoms, including current disease stage, were assessed by neurologists using the Unified Parkinson’s Disease Rating Scale (UPDRS) (18). PD-specific palliative symptoms were measured by the Edmonton Symptom Assessment System Revised: Parkinson Disease (ESAS-rPD) (19).
Statistical analyses
Means and standard deviations were calculated for descriptive variables. Spearman or Kendall Tau correlations between total FACIT scores and continuous or ordinal demographic variables (age, disease duration, education categories, and income ranges) were determined. For non-ordinal categories, or when only a few categories existed, ANOVA type methods were considered. FACIT totals as well as Meaning, Peace, and Faith subscales were run in a Spearman correlation matrix with the following instruments: PDQ-39, HADS Anxiety, HADS Depression, PROMIS-29, McGill QOL, QOL AD, ESAS PD, MDS UPDRS 3, MoCA, Prolonged Grief PG 12, and the Palliative Performance Scale. Partial correlation was used to control for study site, age, sex, disease duration, presence of caregiver, involvement in support groups, education level, income, and cognitive status. Scale scores when items were missing were imputed using the half rule when applicable.
Results
Patient characteristics
Two-hundred and ten PD patients participated in the study, and over 83% (n=175) had a caregiver. Mean patient age was 70.11 years (SD =8.15), and a majority of the sample (n=135, 64%) was male. Approximately 91% (n=159) of patients who had caregivers lived in the same household with them. Complete demographic data for the sample are detailed in Table 1.
Full table
Correlates of spiritual well-being
Total FACIT score was available on 203 patients, and mean total FACIT score was 39.88 out of 60 (SD =9.64), with higher scores indicating greater spiritual well-being. With a total possible score of 20 for each subscale, patients reported average scores of 15.11 (SD =3.20, N=203) for Meaning, 12.87 (SD =3.42, N=203) for Peace, and 11.89 (SD =4.88, N=200) for Faith. Table 2 presents participant means and standard deviations for FACIT scores as well as the other outcome measures included in the study.
Full table
As presented in Table 3, spiritual well-being was positively correlated with older age, existence of a caregiver, involvement in support groups, and, to a lesser degree, income greater than $25,000. Poorer spiritual health was associated with impairment in QOL (PDQ-39), increased anxiety (HADS Anxiety), increased depression (HADS Depression), increased non-motor symptoms (PROMIS-29), increased palliative symptoms (ESAS-PD), and prolonged grief (Prolonged Grief PG 12) (Table 4). Increased spiritual well-being was positively correlated with higher QOL as measured through the McGill QOL and Quality of Life AD scales. There was no association between patient FACIT scores and the MDS UPDRS or MoCA scores. There was no correlation between spiritual well-being and the ESAS-rPD in bivariate analyses; however, after controlling for potential confounders (age, sex, disease duration, involvement in support groups, education, income, and MoCA), higher levels of spirituality was associated with lower symptom burden as measured by the ESAS-rPD (r=−0.38, P<0.0001).
Full table
Full table
Caregiver spirituality was positively correlated with patient spirituality, r[168]=0.34, P<0.0001. Participants with a caregiver had significantly higher spiritual well-being (106.90, SD =316.00) than participants without caregivers (78.49, SD =316.00).
Multivariate analyses indicated consistent trends between variables and the FACIT subscales; however, for all analyses, the Faith subscale had weaker associations with mood and QOL variables than Peace and Meaning.
Relationship between spiritual well-being and QOL
Less patient spiritual wellbeing was associated with greater impairment in QOL, as measured by the PDQ-39 (r=−0.41, P<0.0001). This remained true for all FACIT subscales; however, the Faith subscale (r=−0.24, P=0.002) had a weaker correlation than Peace (r=−0.48, P<0.0001) and Meaning (r=−0.41, P<0.0001). For QOL as measured by the PROMIS-29, overall FACIT (r=−0.49, P<0.0001) as well as subscale scores for Meaning (r=−0.44, n=170, P<0.0001), Peace (r=−0.54, P<0.0001), and Faith (r=−0.29, P=0.0002) mirrored associations with the PDQ-39. On both the McGill and QOL AD, higher scores indicate better QOL. Association trends between spiritual well-being and QOL remain consistent for these measures, with the strongest associations exhibited in the McGill QOL. The FACIT summary score was positively associated with QOL on the McGill (r=0.63, P<0.0001), as were subscales Meaning (r=0.62, P<0.0001), Peace (r=0.63, P<0.0001), and Faith (r=0.40, P<0.0001). Associations with the FACIT summary score (r=0.46, P<0.0001), Meaning (r=0.37, P<0.0001), Peace (r=0.55, P<0.0001), and Faith (r=0.33, P<0.0001) were slightly weaker with the QOL AD.
Discussion
Although previous research has qualitatively acknowledged the presence of a relationship between spirituality and Parkinson’s disease management, this is the first known study to thoroughly detail the relationship between several domains of spirituality and the physical, mental, and palliative symptoms of PD as measured by standardized instruments. Although physical symptoms were not related to FACIT-Sp scores, enhanced patient spiritual well-being was associated with less anxiety and depression. This contrasts with a previous study on spirituality and mood in PD using the Royal Free Interview (RFI) measure documenting no correlation between these variables (20). This discordance may reflect varied nuances between the measures, indicating that the FACIT may better capture spiritual and religious factors specifically associated with PD.
This study is unique in that it examines these relationships by subdomains of spirituality—Meaning, Peace, and Faith—in a group of persons with PD. Previous research examining these subdomains with cancer patients noted that Peace was only correlated with mental health (21); meaning correlated with both physical and mental health measures; and faith had a negative association with mental health (10). Our results differ in that all three subscales had positive associations with mental health and actually no association with physical symptoms as measured through the MDS UPDRS. Although Faith had weaker associations with measures than the other subscales, it was still positively associated with better mental health and QOL, in contrast with a previous study in cancer patients. In the case of all three subscales, higher spirituality was associated with improved QOL despite marked motor impairment as measured by the MDS-UPDRS.
Robust research in oncology populations has long noted a relationship between spiritual well-being and health-related QOL. Delving further, one study found that spiritual well-being had a negative association with specific coping and adjustment styles, such as helpless/hopeless, anxious preoccupation, and avoidance, and it was positively associated with fatalism and a fighting spirit (22). A separate study in mixed long-term chronic illnesses in an Australian population noted the same positive trends between subscales and health-related QOL as the present study, and they also found that Meaning and Peace components were more strongly related to QOL than Faith (23). Their results indicated that employing a fatalistic coping style (e.g., accepting the diagnosis or stoic acceptance) in cancer treatment was positively correlated with Faith while being negatively associated with Meaning and Peace.
Some research indicates that religiosity in PD may be influenced through biological neurocognitive mechanisms affected by the disease (24); however, present findings indicate that the relationship between spirituality and PD is even more complex than previously understood. In addition to correlations with mood, increased spirituality was related to fewer non-motor symptoms and palliative symptoms, and reduced prolonged grief. Findings suggest we may be able to employ patient spirituality through meaning-making and peace to aid in reducing prolonged grief and to enhance patient coping with non-motor symptoms. These complex correlations with physical symptoms, mood, and cognitive factors allude to a multifaceted relationship between spirituality and health in PD, requiring additional research for a more comprehensive understanding of how spirituality can enhance patient care and coping in PD.
Limitations
The primary limitation of the present study is its cross-sectional design, preventing the determination of causality in the clinical relationships discussed. Despite this, these data support a growing evidence base of the relationship between spiritual well-being and the health, mood, and QOL of PD patients, and they highlight the importance of including spiritual support on interdisciplinary and palliative care teams.
One of the original objectives of this study was to examine predictors of spiritual distress, which is defined by a FACIT-Sp score of ≤12 (25). However, this aim could not be addressed, as the lowest FACIT-Sp score for patients was 16, and the lowest for caregivers was 21. Therefore, no spiritually distressed patients or caregivers were included in the sample or analyses. This narrow range of FACIT-Sp scores may subsequently limit the generalizability of findings to patients experiencing significant spiritual distress, and additional research is needed to better understand the predictors of poor spiritual wellbeing for palliative PD patients experiencing it.
Conclusions
The present study supports a growing body of literature emphasizing a relationship between spirituality and health, and understanding this association is particularly important for practitioners working with chronic illnesses, such as PD. Religion and spirituality may influence medical decision-making as well as patient coping strategies and attitudes (26). These results highlight the influences of spirituality in PD management, particularly the relationship between Meaning, Peace, and Faith and mood, palliative symptoms, and QOL.
A critical finding of this study is that spirituality may mitigate some of the physical and non-motor symptoms of PD (including anxiety and depression), and may result in enhanced QOL. As our field is researching pharmacologic means of treating these symptoms, spiritual assessments and supports may prove an empowering resource for patients in their treatment that is consistent with patient values and with little risk. Based on this evidence, clinicians treating individuals with PD should consider spiritual assessments in their practice and should provide patients with access to spiritual counselors experienced in helping those with chronic medical conditions when possible. These data further support the holistic, interdisciplinary care provided to PD patients through palliative care teams offering chaplaincy support to patients.
Acknowledgments
Funding: Research reported in this publication was funded through a Patient-Centered Outcomes Research Institute (PCORI) Award (IHS-1408-20134). All statements in the publication are solely the responsibility of the authors and do not necessarily represent the views of the PCORI, its Board of Governors or Methodology Committee.
Footnote
Conflicts of Interest: The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. Institutional ethics review board approval was received for each of the three study sites (IRB 15-0814). Written informed consent was obtained from the patient for publication of this manuscript and any accompanying images.
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