None listed
Conditions
Brief summary
This aim of this study is to evaluate the effects of acupressure on sleep quality of older persons living in residential care, within Australian context. Study participants will be older persons receiving services from aged care facilities and retirement village. They will be randomly assigned into intervention and control groups. The intervention group will receive acupressure (12-minute/session) three time a week for four weeks. Control group will receive routine care only. The primary outcome measures is sleep quality. The secondary outcomes are depression, anxiety and quality of life. The baseline data will be collected before commencing acupressure intervention (T0), followed by 4-week acupressure sessions. The outcome data will be collected at the end of intervention (T1) and two weeks after the intervention (T2).
Interventions
The intervention involves 12-minute acupressure sessions, three times a week for four weeks. Acupressure technique is application of finger or thumb pressure for 2 minutes on each acupoint (acupuncture point) using circular motion. The selected acupoints are HT7, PC6 and SP6; located on both wrists, hands, and calves. The time for acupressure will be scheduled in the morning or afternoon (from 9am – 5pm), at a convenient time for the participants. Acupressure will be performed by the PhD student researcher, who has career background in general nursing, hemodialysis and nursing education. She attended acupressure practitioner training in Sydney, Australia. One of the supervisors of the PhD student researcher is a qualified acupressure practitioner. She has supervised the design and implementation of the acupressure intervention. This dosage is based on the findings of systematic and integrative reviews (Hmwe et al., 2018; Hmwe et al., 2016; Waits et al., 2016). For the present study, acupressure intervention protocol has been developed based on TCM concepts, literatures including reviews (Hmwe et al., 2016; Hmwe et al.; 2018; Huang et al., 2009; Waits et al., 2016), research evidences (Lai et al., 2017; Lu et al., 2013; Reza et al., 2010; Zeng et al., 2016), and consultation with qualified specialist in acupressure (one of the PhD supervisors). To maintain fidelity of the intervention, student researcher will adhere to the acupressure intervention protocol. She will keep field note records, which include date and time of acupressure sessions, and observation on participants' general condition during each acupressure session. The supervision team will monitor the performance of student researcher.
Sponsors
Study design
Eligibility
Inclusion criteria
i) aged 65 and above, ii) a resident of an aged care facility or a retirement village iii) self-reported poor sleep quality, iv) able to communicate with researcher in response to questionnaires, and v) give informed valid consent to participate in the study
Exclusion criteria
i) severe cognitive impairment (MMSE score 9 or less), ii) amputation of upper or lower limbs because acupressure will be applied on both hands and legs, iii) recent fracture on forearm or on the leg, iv) severe illness, presence of bleeding disorder such as haemophilia, or blood clotting disorders such as thrombophlebitis to avoid potential complications, v) current treatment on blood thinning drugs, and vi) inflammation, skin infection or lesions near selected acupoints. Level of cognitive impairment will be identified based on Mini-Mental Health Status (MMSE) record in the respective care unit. The MMSE score less than or equal to 9, will be considered as severe cognitive impairment in older population (Molloy et al., 1991; Molloy and Standish, 1997).