Older Adults Clinical Trial
Official title:
The Development and Validation of the Arabic Otago Exercise Program: A Feasibility Controlled Study
Verified date | April 2023 |
Source | University of Jordan |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Falls are common in older adults and may lead to disability or even death. Therefore, exercise programs that focus on preventing falls by improving strength and balance are important to investigate in older adults. One of the home-based exercise programs that was found effective in reducing the risk of falling and the rate of subsequent falls in older adults is the Otago exercise program (OEP). The OEP is an individualized home based retraining program that works mainly on balance and lower extremity strength through several progressive resistive exercises. The OEP is available in English language since late 1990. However, its use in the Arabic-speaking countries is limited due to the language barrier. Therefore, translating such a program to the Arabic language would facilitate its use among Arabic-speaking older adults. Therefore, this study aims: - To translate the Otago Exercise Program (OEP) into the Arabic language. - To assess the feasibility of the Arabic OEP in a pilot sample of Arabic-speaking older adults.
Status | Completed |
Enrollment | 20 |
Est. completion date | December 31, 2022 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 60 Years and older |
Eligibility | Inclusion Criteria: - Adults who are 60 years of age and older. - Who can read and write in Arabic language. - Who are able to walk outdoors with no more support than a single point cane. Exclusion Criteria: - Who have a serious orthopedic condition (e.g., recent lower limb surgery, severe arthritis of a lower limb) or major neurological disorder (e.g., stroke with unilateral or bilateral paresis, Parkinson disease or multiple sclerosis) that could restrict functional mobility. - Who are unable to comprehend study information and consent processes due to any illness including dementia. |
Country | Name | City | State |
---|---|---|---|
Jordan | University of Jordan | Amman |
Lead Sponsor | Collaborator |
---|---|
University of Jordan |
Jordan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of Falls in the previous 12 months | Incidence of Falls and Falls Circumstances in the previous 12 months | Previous 12 months | |
Primary | Incidence of falls during the treatment period (8 weeks) | Incidence of falls during the treatment period (previous 2 months) to assess the effect of the intervention on the incidence of falls. | Immediately post intervention. | |
Secondary | Fear of Falling (using the Falls Efficacy Scale-International) | The effect of the intervention on fear of falling. The total score ranges between 16 and 64 with a higher score indicates greater fear of falling (worse). | Immediately post intervention. | |
Secondary | Balance (using Chair balance test and Four test balance scale) | The effect of the intervention on balance. The time taken to conduct these balance tasks are timed using a stopwatch. The longer the time taken by the participant to perform the tasks, the worse the balance. There is no minimum or maximum scores for these tests. | Immediately post intervention. | |
Secondary | Mobility (using Timed-Up and go) | The effect of the intervention on mobility. This assessments of mobility is timed out using a stopwatch. | Immediately post intervention. | |
Secondary | Grip strength (using a hand held dynamometer) | The effect of the intervention on grip strength. The strength of Hand grip muscle will be assessed using a dynamometer in kilograms. | Immediately post intervention. | |
Secondary | The Quality of Life (using Medical Outcomes Study Short Form 12) | The effect of the intervention on Quality of Life. The total score ranges between 0% to 100% with higher score indicates a better quality of life (better). | Immediately post intervention. | |
Secondary | The severity of Anxiety and Depression (using Hospital Anxiety and Depression Scale) | The effect of the intervention on the severity of Anxiety and Depression. The total score for each subscale of the HADS ranges from 0 to 21 with higher score indicates more severe anxiety or depression (worse). | Immediately post intervention. | |
Secondary | Pain (using pain rating scale) | The effect of the intervention on pain. The total score of PRS ranges between 0 to 10 with higher score indicates more pain and interference with discomfort (worse). | Immediately post intervention. | |
Secondary | The severity of fatigue (using the Modified Fatigue Impact Scale) | The effect of the intervention on fatigue. The total score of MFIS ranges between 0 to 84 with higher score indicates higher impact of fatigue on on daily functioning (worse). | Immediately post intervention. |
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