Effect of Massage Therapy in a Multisensory Environment for Intellectual Disabilities
- Conditions
- Muscle HypotoniaBehavior Disturbance
- Interventions
- Behavioral: Multisensory environment (MSE)Behavioral: Massage therapy (MT)Other: Control groupBehavioral: Massage therapy in multisensory environment (MT-MSE)
- Registration Number
- NCT02120820
- Lead Sponsor
- The Hong Kong Polytechnic University
- Brief Summary
The aim of this study is to evaluate the effectiveness of multisensory environment (MSE) and/or massage therapy (MT) in residents with severe and profound intellectual disabilities (ID) who received massage therapy in MSE, activities in MSE alone, massage therapy in usual care environment, or usual care with attention.
Since there has not yet been any conclusive evidence to show the clinical efficacy of MT and MSE on relaxation and reducing challenging behaviours, the following null hypotheses are suggested:
1. There will not be any differences on reducing heart and respiration rates between MT-MSE, MT, MSE, and usual care only over the 10-week intervention period and a 2-week follow-up.
2. There will not be any differences on adaptive behaviours and levels of alertness between MT-MSE, MT, MSE, and control group over the 10-week intervention period and a 2-week follow-up.
3. There will not be any differences on frequency and severity of challenging behaviours between MT-MSE, MT, MSE, and control group over the 10-week intervention period and a 2-week follow-up.
- Detailed Description
Design:
This study adopts a mixed methods research design, in which both quantitative (i.e., randomized controlled trial design) and qualitative (exploratory) approaches will be used.
Methods:
After the study criteria are checked and met and proxy consent has been obtained, the participants will undergo a period of washout (4 weeks) from the current multisensory environment (MSE) and/or massage therapy (MT) sessions. After that, the baseline measurement of all outcome measures will be taken. All of them will then be randomly assigned to one of the four study groups, including three treatment groups, namely massage therapy in MSE (MT-MSE), MSE only and massage therapy in usual care environment (MT), and one control (routine care) group.
The effects of the three proposed interventions and routine care only groups on the study outcomes, including frequency and severity of challenging behaviour, adaptive behaviour, alertness level, and heart and respiration rate, will be compared between groups at baseline, interim (i.e., 5 weeks after the interventions started), immediately after completion of the interventions (i.e. 10 weeks after the interventions started), and 2 weeks follow up (i.e. at 12 weeks from the start of intervention, but no intervention at week 11 and 12). A pilot study will be conducted to review the feasibility and clarity of the study procedure, intervention protocols, and outcome measurements in around 30 patients with similar clinical characteristics (i.e., 8 subjects per groups) before starting the main study.
Primary outcomes of the study are frequency and severity of challenging behaviours, and the physiological signs (i.e., respiration and pulse rate). The secondary outcomes are the levels of alertness and adaptive behaviours.
Primary nurses who are responsible to formulate the individualized MSE and/or MT programs of the participants in the three treatment groups will be invited to participate a face-to-face semi-structured interview in order to explore their perceptions and opinions towards the strengths and limitations of the intervention(s) used, factors influencing the challenging behaviours of the disabled residents, and their suggested strategies in reducing their clients' challenging behaviours in their work setting.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 240
- exhibiting at least one type of challenging behavior
- admitted at least 3 months for long-term care
- being dependent on nursing care and physical assistance in daily activities
- aged 18 to 64 years
- seriously ill or completely bed-rest residents
- having infectious diseases
- frequently discharged to general hospital for acute care
- frequent home or day leave
- having pressure ulcer and/or severe contracture and deformity
- being restless and reluctant to stay in multisensory environment, or receive massage therapy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Multisensory environment Multisensory environment (MSE) Multisensory environment (MSE): 30 minutes/session, twice a week for 10 weeks Massage therapy Massage therapy (MT) Massage therapy (MT): 15 minutes/session, twice a week for 10 weeks Control group Control group Control group: usual care for 10 weeks, with attention and interactions with the caregivers only. Massage in multisensory environment Massage therapy (MT) Participants receive 15 minutes massage therapy in multisensory environment (MT-MSE), twice a week for 10 weeks. Massage in multisensory environment Multisensory environment (MSE) Participants receive 15 minutes massage therapy in multisensory environment (MT-MSE), twice a week for 10 weeks. Massage in multisensory environment Massage therapy in multisensory environment (MT-MSE) Participants receive 15 minutes massage therapy in multisensory environment (MT-MSE), twice a week for 10 weeks.
- Primary Outcome Measures
Name Time Method Behavior Problem Inventory (BPI-01): frequency and severity of challenging behaviours Baseline (at recruitment) BPI-01 consists of 49 items with three subscales and has been widely employed in people with intellectual disability who are living in residential settings. This instrument is to evaluate the frequency and severity of challenging behaviours over the past two weeks of each assessment time points.
Each item of the scale can be assessed on both frequency and severity of each kind of behaviour. The frequency scale is a 5-point rating scale: 0 - never, 1 - monthly, 2 - weekly, 3 - daily, and 4 - hourly. The severity scale is a 4-point Likert scale, denoted by: 0 - no problem, 1 - a slight problem, 2 - a moderate problem, and 3 - a severe problem. If a resident does not exhibit any behaviour listed in the item, "never" and "no problem" should be rated on that item.Behavior Problem Inventory (BPI-01) 12 weeks after intervention started (Post-test 2) Behavior Problem Inventory (as described above) will be used to measure the frequency and severity of challenging behaviours by the end of week 12.
Respiration and Pulse Rate 12 weeks after intervention started (Post-test 2) Respiration rate and heart (pulse) rate will be measured 3 minutes by the end of week 12. Their average values will be used for outcome analysis.
- Secondary Outcome Measures
Name Time Method Alertness Observation Checklist (AOC) 12 weeks after intervention started (Post-test 2) Alertness Observation Checklist (AOC) will be used to measure the average amount of the four levels of alertness by the end of week 12.
Behaviour Checklist (BC) 12 weeks after intervention started (Post-test 2) Behaviour Checklist (BC) will be used to measure the frequency of self-stimulating and adaptive behaviours by the end of week 12.
Trial Locations
- Locations (1)
Siu Lam Hospital
🇭🇰Tuen Mun, New Territories, Hong Kong