Live Research Spotlight 12: Sleep, Quality of Life, & Physical Health
mHealth Sedentary Reduction Program in Older Adults with Knee Replacement: Randomized Controlled Trial
Time: 03:00 PM - 03:07 PMTopics: Aging, Physical Activity
Methods: Older adults with knee replacement ≤1 year ago with a smartphone who self-reported spending ≥7 hours/day sitting were randomized to either an mHealth sedentary reduction program (NEAT!2) or an attention control group. NEAT!2 was guided by the Dual-Process Theory and targeted both automatic (implicit) and controlled (conscious) processes. NEAT!2 participants received an app that triggers notifications to stand up after ≥20 min of inactivity as well as 5 coaching calls which included goal setting and problem-solving around reducing sedentary time. The Control group received an app focused on knee replacement pre- and post-operative and 5 coaching calls discussing topics not related to sedentary behavior or physical activity. Multiple linear regression models with GEE adjusted for covariates were used to examine differences and changes in outcomes between groups including objectively-measured sedentary time and physical activity (ActiGraph and activPAL monitors), physical function (6-min walk test, timed up and go, chair stands), and WOMAC pain were assessed at baseline, 2-, and 5 months.
Results: A total of 83 participants were randomized (65.3±9.4 years, 32.7±6.9 kg/m2, 75% female, 77% White) and 98% and 85% of participants completed the 2- and 5-month assessments, respectively. Participants completed 4.8±0.7 calls (out of 5), with no differences between groups. NEAT!2 participants received an average of 10.3±6.1 notifications/day. At baseline, participants spent 73.7±6.8% of waking time in sedentary behavior and 65.2±79.8 min/week in moderate-vigorous activity. There were no group x time differences in sedentary time, physical activity, physical function, or pain at 2- or 5-months.
Conclusions: A brief mHealth sedentary reduction program was not effective at reducing sedentary time among older adults within 1 year of knee replacement. Given this population spends the majority of their day in sedentary behaviors, it is critical to explore individual variability in response as well as develop more intensive programs to determine the optimal way to reduce sedentary time.
Authors:
Author - Christine Pellegrini, PhD, FSBM,
PhD, FSBM,
University of South Carolina
Co-Author - Sara Wilcox, PhD, FSBM,
PhD, FSBM,
University of South Carolina
Co-Author - Jungwha Lee,
PhD,
Northwestern University
Co-Author - Katherine E. DeVivo,
University of South Carolina
Co-Author - Jeffrey Hopkins,
MD,
Prisma Health
Co-Author - Scott Jamieson,
University of South Carolina
Co-Author - Kailyn Horn,
University of South Carolina
Self-Acupressure’s Impacts on Physical Functioning Among Black and Latina Breast cancer Survivors: Preliminary Results from A Pilot Randomized-Controlled Trial
Time: 03:07 PM - 03:14 PMTopics: Integrative Health and Spirituality, Cancer
We conducted a pilot Randomized-Controlled Trial (RCT) of a culturally adapted SA training video in English and Spanish. BCS diagnosed at stage 0-IV with limited physical functioning at baseline were randomized 2:1 to either the SA intervention or Usual Care (UC, a BCS fact sheet). The SA group learned SA for three acupoints daily (6 mins total) in an educational video and live training. We enrolled 47 BCS of whom 34 completed baseline (T0) and an 8 week follow-up (T1; 18 Black, 16 Latina; age Mean [M] = 54.55; 72.35% retention; n=21 in SA, n=13 in UC). The PROMIS 6-item short form assessed physical functioning. Preliminary analysis of SA impact on physical functioning was assessed with between and within group t-tests. We also explored whether the SA impact differed between BCS with high (at least 75% of days practiced) and low engagement in SA as documented by daily logs.
The SA group and UC group’s demographics and baseline physical functioning did not significantly differ, but SA experienced more symptoms (M=20) at baseline than UC (M=13). However, the SA group (mean difference; MD=1.90, p=0.07) improved their physical functioning from T0 to T1 slightly more than the UC group (MD=1.07, p=0.19). The improvement between the two groups was not significantly different. Within the SA group, the 13 BCS (62%) with high SA engagement (vs. 8 low) had clinically significant increases in physical functioning (MD=3.37) relative to low engagement (MD=-0.50).
This pilot RCT demonstrated the initial feasibility of SA for Black and Latina BCS who engaged in SA practice. The limited difference between SA and UC in physical functioning may have been impacted by 38% of the SA group having low SA engagement in practice, highlighting a need for targeting engagement in future trials. We are currently conducting interviews with BCS to gather feedback about maximizing engagement in a future RCT.
Authors:
Author - Katarina E. AuBuchon, PhD,
PhD,
Georgetown Lombardi Comprehensive Cancer Center
Co-Author - Kristi D. Graves, PhD, FSBM,
PhD, FSBM,
Georgetown University
Co-Author - Suzanne Danhauer,
MD,
Wake Forest University School of Medicine
Co-Author - Jae Eun Chung,
PhD,
Howard University
Co-Author - Emily Cramer, PhD,
PhD,
Howard University
Co-Author - Lourdes Inbar-Albo,
MA,
Georgetown Lombardi Comprehensive Cancer
Co-Author - Amrita Bonthu,
BA, MA,
Georgetown Lombardi Comprehensive Cancer
Co-Author - Ella Lowry,
Georgetown Lombardi Comprehensive Cancer
Co-Author - Carla Arieta,
Effective Integrative Healthcare
Co-Author - Dingyue Yang,
Georgetown Lombardi Comprehensive Cancer
Co-Author - Jacqueline Chen,
Georgetown Lombardi Comprehensive Cancer
Co-Author - Sophia Urdinola,
Georgetown Lombardi Comprehensive Cancer
Co-Author - Claudacia Clemmons,
Georgetown Lombardi Comprehensive Cancer
The MATCH Study: Mindfulness and Tai Chi for Cancer Health. Primary Results of a Comparative Effectiveness Trial
Time: 03:14 PM - 03:21 PMTopics: Integrative Health and Spirituality, Cancer
Methods: The design was a pragmatic preference-based multi-site randomized comparative effectiveness trial. Participants with a preference for either MBCR or TCQ received their preferred intervention, while those without a preference were randomized into either program. Further, within the preference and nonpreference groups, participants were randomized 2:1 into immediate intervention or wait-list control. Group interventions were delivered in-person in cohorts of up to 20 participants, over 9-11 weeks. Profile of Mood States (POMS) Total Mood Disturbance (TMD) scores post-intervention were the primary outcome, with 6 POMS subscales also investigated.
Results: 587 participants were enrolled, 75% females. Average age was 60.7 years, with 12 different cancer types represented. Half were diagnosed at stage I - II (50.1%), 64% had a preference, of TCQ (213; 57% of those with a preference) and MBCR (163; 43%), and the remaining 36% with no preference were randomized equally to either program. Both randomized MBCR (p=0.0173) and TCQ (p=0.0135) groups showed significantly more improvement on the POMS TMD scores than their respective waitlists, but the preference groups did not. Both MBCR and TCQ (whether randomized or chosen) significantly reduced the subscale of anger, only TCQ reduced depression and improved vigor, only MBCR improved tension-anxiety, and neither intervention significantly reduced confusion or fatigue subscales. Effect sizes were small to medium.
Conclusions: Both active interventions improved overall mood disturbance compared to control in this large, broad pragmatic sample of cancer survivors, and the role of program preference was minor. MBCR was more effective for reducing anxiety, while TCQ was more effective for depression and vigor. A wide range of secondary outcomes and biomarker data has yet to be reported, which will further characterize the differential effects of these two therapies.
Authors:
Co-Author - Jennifer Jones,
PhD,
University Health Network/University of Toronto
Co-Author - Devesh Oberoi,
MD PhD,
University of Calgary
Co-Author - Katherine-Ann Piedalue,
BSc,
Memorial University
Co-Author - Peter Wayne,
PhD,
Harvard University
Co-Author - Oluwaseyi Lawal,
PhD,
University of Calgary
The Temporal Dynamics of the Association between Daily Physical Activity and Life Satisfaction
Time: 03:21 PM - 03:28 PMTopics: Physical Activity, Quality of Life
Authors:
Author - Steriani Elavsky, PhD,
PhD,
University of Ostrava
Co-Presenter - Marek Brabec, PhD,
Institute of Computer Science, The Czech Academy of Sciences
Co-Author - Lenka Knapova,
University of Ostrava
Co-Author - Barbora Kastovska,
University of Ostrava
Co-Author - Michal Sebera,
University of Ostrava
Co-Author - Vera Kristyna Jandackova,
University of Ostrava
Co-Author - Misha Pavel, BS, MSEE, Ph.D.,
BS, MSEE, Ph.D.,
Northeastern University
Association Between Insomnia Symptom Trajectories and Cognitive Decline in Older Adults with Subjective Cognitive Decline
Time: 03:28 PM - 03:35 PMTopics: Sleep, Aging
Methods: Data from six waves of the Health and Retirement Study (2010–2020) were analyzed. The study sample included 1,376 community-dwelling older adults aged 50 and above who had SCD at baseline and at least three waves of cognitive performance data. SCD was determined by self-reperceived memory decline without objective cognitive impairment (Modified Telephone Interview for Cognitive Status [TICS-M]>11) and no diagnosis of Alzheimer’s disease or dementia. Growth mixture modeling was used to identify classes of trajectories of insomnia symptoms based on the count of four symptoms from the Jenkins Sleep Scale. A multi-level modeling then examined the association between insomnia trajectory classes and cognitive performance (TICS-M scores) over the 10-year period, adjusting for sociodemographic and health-related variables.
Results: Four distinct insomnia symptom trajectories were identified among older adults with SCD: Minimal Insomnia Symptoms–Stable (76.1%); Low Insomnia Symptoms–Increasing (10.8%); Moderate Insomnia Symptoms–Decreasing (8.0%); and High Insomnia Symptoms–Stable (5.1%). The multi-level model revealed that older adults with SCD in the "Low Insomnia Symptoms–Increasing" class experienced a significantly faster rate of cognitive decline compared to those in the " Minimal Insomnia Symptoms–Stable" class (estimate = -0.25, 95%CI = -0.38, -0.12).
Conclusion: Increasing insomnia symptoms over time may be associated with faster cognitive decline. The importance of monitoring insomnia symptoms was highlighted in older adults with SCD. Early evaluation and intervention of insomnia symptoms may potentially mitigate cognitive decline in this at-risk population.
Authors:
Presenter - Jing Huang,
MPhil,
Johns Hopkins University School of Nursing
Co-Author - Nancy A. Perrin,
PhD,
Johns Hopkins University School of Nursing
Co-Author - Chakra Budhathoki,
PhD,
Johns Hopkins University School of Nursing
Co-Author - Sarah L. Szanton,
PhD,
Johns Hopkins University School of Nursing
Co-Author - Junxin Li,
PhD,
Johns Hopkins University School of Nursing
Discrimination relating to sexual identity is associated with increased sleep disturbance and daytime dysfunction from tiredness in older sexual minority men in New York City
Time: 03:35 PM - 03:42 PMTopics: HIV/AIDS, Health of Marginalized Populations
A growing evidence base is recognizing the deleterious effects of discrimination experiences on sleep health. Our study explores how experiences of discrimination related to one’s sexual identity is associated with global sleep health indicators in a sample of older sexual minority men living in New York City. We hypothesized that greater discrimination scores on the Everyday Discrimination Scale (adapted for sexual identity discrimination) would be associated with worse scores on sleep health.
Method:
Utilizing baseline data from an observational study, our 82 participants were NYC-based, older (50+) sexual minority men living with HIV. Measures included: the 10-item Everyday Discrimination Scale adapted to assess experiences in day-to-life of being treated badly or unfairly due to sexual identity status, and the Pittsburgh Sleep Quality Index administered in-office via an online Qualtrics survey. Multiple linear regressions, adjusting for age and race/ethnicity (dichotomized as Black/Latino or White) tested the association between discrimination and each of the PSQI’s sleep components: sleep quality, duration, latency, efficiency, disturbance, and daytime dysfunction.
Results:
Bivariate correlations showed significant associations between greater discrimination and two of the sleep components: greater sleep disturbance (r=.23, p= .037) and daytime dysfunction (r=.30, p= .006). In multivariable analyses adjusting for age and for race/ethnicity, greater discrimination was associated with greater sleep disturbance (B=0.02, p=.026), and with worse daytime dysfunction due to tiredness (B=0.03, p=.003).
Discussion:
We found that everyday experiences of sexual identity-related discrimination linked to greater past-month sleep disturbance and daytime dysfunction due to tiredness in a sample of older SMM living with HIV. This highlights the increasingly recognized negative impact of discrimination and stigma on sleep health, the sequalae of which include poorer immune functioning, poorer cardiovascular health, and poorer mental health, in an already vulnerable population. Reducing societal discrimination related to sexual identity has vital importance for improving and maintaining the health of sexual minority individuals more broadly. This contributes to the growing evidence base highlighting discrimination as a biopsychosocial hazard.
Authors:
Co-Author - Carly Wolfer,
MA,
Graduate Center of City University of New York (CUNY)
Co-Author - Patrick George, III,
MSSR,
Albert Einstein College of Medicine
Co-Author - Hannah (Hyejin) Park,
MSc,
Rutgers University
Co-Author - K. Marie Sizemore,
PhD,
Rutgers University / Robert Wood Johnson Medical School
Co-Author - Devin English, PhD,
PhD,
Rutgers University
Live Research Spotlight 12: Sleep, Quality of Life, & Physical Health
Description
Date: 3/28/2025
Start: 3:00 PM
End: 3:50 PM
Location: Franciscan A