A Dyadic e-Health System on Enhancing Healthy Lifestyles of Older Adults With Sarcopenia
Sarcopenia
About this trial
This is an interventional treatment trial for Sarcopenia focused on measuring Sarcopenic Obesity, e-Health System, Family-oriented Nutritional Intervention, Exercise, RCT
Eligibility Criteria
Inclusion Criteria: Community-dwelling older people aged > 60 years; Meeting the diagnostic criteria of sarcopenia according to the Asian Sarcopenia Working Group (ASWG): Early-stage sarcopenia refers to the fulfillment of one of the following criteria: low handgrip strength < 28 kg for men and < 18 kg for women, low muscle quality as reflected by low appendicular skeletal muscle mass (ASM) /height squared < 7 kg/m2 for men and <5.7 kg/m2 for women, or low physical performance with a Short Physical Performance Battery (SPPB) score of < 9; Able to communicate, read, and write in Chinese without significant hearing and vision problems to ensure that our instructions are understood; Own a smartphone, and able to access the internet at home or elsewhere; Reside with family and have at least one daily shared meal (family is defined as an individual who has a significant personal relationship with the participant, such as next of kin, spouse and the individual must be at aged > 18); and Able to identify a family member who has a smartphone and is willing to support the participant to use the e-Health System. Exclusion Criteria: With any form of disease or condition that might affect food intake and digestion (such as severe heart or lung diseases, diabetes, cancer, or autoimmune diseases); Currently suffering from acute gouty arthritis or had a gout attack in the past year; Taking medications that may influence eating behaviour, digestion, or metabolism (such as weight loss medication); Being addicted to alcohol, which might affect the effort to change dietary behaviour; Having impaired mobility, which might affect participation in exercise training, as defined by a modified Functional Ambulatory Classification score of < 7; Having renal impairment, based on the renal function blood test which will be screened by a geriatrician; Having depressive symptomatology, defined by a Geriatric Depression Scale score of > 8; Suffering from dementia (i.e., MoCA<20 or clinical dementia rating ≥1); Having any medical implant device such as a pacemaker, because low-level currents will flow through the body when doing the bioelectric impedance analysis (BIA by InBody S10, Korea), which may cause the device to malfunction.
Sites / Locations
- The Hong Kong Polytechnic Universtiy
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
The Experimental Group
The Control Group
Participants in the Experimental Group will attend an implementation program guided by the Self-Determination Theory (SDT). The 12-week intervention consists of a 4-week, group-based, face-to-face supervised sessions conducted by a well-trained Research Assistant, plus an 8-week self-management phase.
Participants in The Control Group will attend 4-weekly, group-based, regular face-to-face health talks about managing sarcopenia with the exact dosage provided to the intervention group.