- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05002803
The Development and Validation of the Arabic Otago Exercise Program
The Development and Validation of the Arabic Otago Exercise Program: A Feasibility Controlled Study
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.
Study Overview
Detailed Description
- Research ethics: This study got the ethics approval from the IRB at Jordan University Hospital at University of Jordan. A consent form that contains the study procedures will be prepared and signed from all participants. To insure the privacy of participants, every older adult will be assigned a study identification number. All results will be stored in a locked cabinet/computer only accessible by the researchers.
- Participants: Data will be collected prospectively from older adults in Jordan. Older adults will be approached to complete the program via Jordan University Hospital, community based organizations (e.g. Help-Age International Jordan) and social media platforms such as Facebook and WhatsApp.
Design:
Phase 1: Translation and cultural adaptation of the Otago Exercise Program (OEP) into the Arabic language.
- The permission of translating the program will be granted from its developers.
- English version of the program will be translated into the Arabic language in accordance with the World Health Organization (WHO) forward/backward translation protocol (https://www.who.int/substance_abuse/research_tools/translation/en/ ).
- An Arabic booklet of the OEP will be prepared.
Phase 2: Assessing feasibility of the OEP on a pilot sample of Arabic-speaking older adults using a focus group and a pilot Trial.
- The Arabic version of the OEP will be sent to an expert panel for review. Suggested changes will be considered and made.
- The Arabic version of the OEP will be sent to 2 groups that consist of 5 older adults each. They will be given sufficient time to go through the exercise manual before being invited to a focus group meeting to discuss the Arabic wording and feasibility of the Arabic version of the OEP.
- A topic guide will be prepared to assess the feasibility and user-friendliness of the Arabic OEP manual.
- The meeting will be recorded after taking their permission and the recording will be transcribed and analyzed.
- If there are major changes to the program, the experts will meet to make the appropriate changes and another focus group will be conducted.
- The final version of the Arabic OEP will be implemented for 8 weeks on a pilot sample of Arabic speaking older adults using a controlled design with 10 older adults in the treatment group and 10 older adults in the control group.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Amman, Jordan, 11942
- University of Jordan
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Control group
Older adults will receive only health awareness videos every 2 weeks.
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Experimental: Otago Exercise Program
Older adults will receive the Arabic Otago Exercise Program for 8 weeks plus health awareness videos.
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A Home-based Exercise Program to improve strength and balance and prevent falls.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Incidence of Falls in the previous 12 months
Time Frame: Previous 12 months
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Incidence of Falls and Falls Circumstances in the previous 12 months
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Previous 12 months
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Incidence of falls during the treatment period (8 weeks)
Time Frame: Immediately post intervention.
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Incidence of falls during the treatment period (previous 2 months) to assess the effect of the intervention on the incidence of falls.
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Immediately post intervention.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Fear of Falling (using the Falls Efficacy Scale-International)
Time Frame: Immediately post intervention.
|
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).
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Immediately post intervention.
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Balance (using Chair balance test and Four test balance scale)
Time Frame: Immediately post intervention.
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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.
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Immediately post intervention.
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Mobility (using Timed-Up and go)
Time Frame: Immediately post intervention.
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The effect of the intervention on mobility.
This assessments of mobility is timed out using a stopwatch.
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Immediately post intervention.
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Grip strength (using a hand held dynamometer)
Time Frame: Immediately post intervention.
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The effect of the intervention on grip strength.
The strength of Hand grip muscle will be assessed using a dynamometer in kilograms.
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Immediately post intervention.
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The Quality of Life (using Medical Outcomes Study Short Form 12)
Time Frame: Immediately post intervention.
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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).
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Immediately post intervention.
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The severity of Anxiety and Depression (using Hospital Anxiety and Depression Scale)
Time Frame: Immediately post intervention.
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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).
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Immediately post intervention.
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Pain (using pain rating scale)
Time Frame: Immediately post intervention.
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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).
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Immediately post intervention.
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The severity of fatigue (using the Modified Fatigue Impact Scale)
Time Frame: Immediately post intervention.
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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).
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Immediately post intervention.
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Other Study ID Numbers
- 2021/134
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
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