- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04063553
Impact of Volunteerism in the Acute Setting
Impact of Volunteerism in the Acute Setting: Guiding Rehabilitative Exercises in Patients After Total Knee Replacement (TKR). A Pilot Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Rehabilitation, with a particular emphasis on physiotherapy and exercise, is widely promoted and strongly recommended after total knee replacement (TKR). The primary goals of rehabilitation are to improve knee range-of-motion, muscle strength, functional mobility and perceived quality of life. Exercises are usually prescribed and guided by a physiotherapist attending to the patient. The intensity of rehabilitation has an impact on clinical outcome. A study done by Lee et al in 2012 concluded that higher exercise dose translates to better function after TKR, especially in older population and for those with higher pain. Various literatures has also strongly recommended twice a day rehabilitation session for patients after TKR (Cook et al, 2008; Smith et al 2012). The standard practice in the in-patient setting is that physiotherapist will attend to the TKR patients once a day and remind patients to perform exercises by themselves, following the exercise booklet given, during their free time in the ward to maximise their recovery. However, due to post-operative fatugue, pain and fearful of movement, most of the patients are not compliant to the exercises given.
Volunteers have been present in health care settings for centuries. Several studies have shown that volunteers can be an essential part of the healthcare system. They are commonly involved in non-clinical tasks such as providing emotional support to patients and families (Burbeck et al., 2014), assisting with meals (Robinson et al., 2014) and facilitating recreational activities in patients with dementia (Hall et al., 2017).
However, no study has investigated the involvement of volunteers in actual clinical work. Our study aim to explore the feasibility of volunteers involvement in teaching and guiding exercises which conventionally done by physiotherapists, and to investigate the effectiveness of such volunteer service. There is no existing evidence on volunteers dealing with elderly patients in acute stage right after surgery as well, and this clinical research will be the first to explore that.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Singapore, Singapore
- Recruiting
- Tan Tock Seng Hospital
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Contact:
- Eng Chuan Neoh, masters
- Phone Number: 91733222
- Email: eng_chuan_neoh@ttsh.com.sg
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Standard unilateral TKR without complications
- 55 years or older
- Pain less than or equal to 6/10 (i.e or between mild to moderate)
- Cognitively intact (able to follow at least 1-step instruction consistently)
- Vitals stable (Blood pressure, HR, oxygen saturation)
- Able to verbalise understanding and give informed consent
- Able to understand Mandarin or English
Exclusion Criteria:
- Unable to follow instructions consistently due to
- Cognitive impairment (Dementia, delirium)
- Behavioural issues (Confused, aggressive)
- Visually or hearing impaired
- Language illiteracy (listening)
- Medically unstable such as Hb drop (< 8) , acute desaturation
- Reduced exercises tolerance- Unable to tolerate a 20 minutes exercise session
- Post-operative complication such as delirium, DVT, cardiac issues.
- Excessive bleeding from the wound dressing
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Other: Intervention arm
Subjects in the intervention group will receive standard physiotherapy care and an additional volunteers session once a day for at least 3 times during their stay in the hospital.
The volunteer will set up the TKR exercise video for the subjects, then supervise or guide the subjects with the exercises.
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Subjects in the intervention group will receive standard physiotherapy care and an additional volunteers session once a day for at least 3 times during their stay in the hospital. The volunteer will set up the TKR exercise video for the subjects, then supervise or guide the subjects with the exercises. All volunteers are recruited from TTSH volunteers pool managed by Center of Health Activation (CHA). TKR volunteers are trained by the study team, including a formal classroom session and a practical and role play session. After the training, volunteers need to pass 3 assessment by the physiotherapists in order to attend to patients independently by themselves. Volunteers who are bilingual will attend to the subject alone, or else those who can only converse in Chinese/ English will pair up with another volunteer who knows another language to make sure there is no communication barrier between volunteers and patients. |
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Other: Control arm
The control group subjects will receive only standard physiotherapy care and they will be instructed to perform 1 set of exercises daily following a brochure given
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. The control group subjects will receive only standard physiotherapy care and they will be instructed to perform 1 set of exercises daily following a brochure given.
The exercises in the brochure and exercises taught by the volunteers are the same.
The video and brochure are available in both English and Chinese version.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee flexion and extension range of motion
Time Frame: through study completion, an average of 5 days
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knee range of motion will be measured using goniometer
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through study completion, an average of 5 days
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Quadriceps strength
Time Frame: through study completion, an average of 5 days
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Quads strength will be assessed by using handheld dynamo-meter
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through study completion, an average of 5 days
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Pain intensity
Time Frame: through study completion, an average of 5 days
|
pain intensity will be assessed by using VAS scale.
VAS scale is a valid scale to assess pain intensity.
It is a likert scale with 0-10 with 0 is no pain and 10 is maximum pain, Subject will be asked to give a number based on the pain level that they feel.
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through study completion, an average of 5 days
|
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Timed up and Go test
Time Frame: through study completion, an average of 5 days
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Functional test to measure the duration needed to complete the task
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through study completion, an average of 5 days
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Length of stay
Time Frame: through study completion, an average of 5 days
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Length of hospital stay to discharge home
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through study completion, an average of 5 days
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survey
Time Frame: through study completion, an average of 5 days
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survey with likert scale 1-5 to investigate patient acceptance and satisfaction level towards volunteer service
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through study completion, an average of 5 days
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quiz
Time Frame: through study completion, an average of 5 days
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quiz with Yes or No to test the knowledge of subjects about post TKR rehab
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through study completion, an average of 5 days
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Eng Chuan Neoh, masters, Senior Physiotherapist
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2018/00638
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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