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The goal of this randomized control trial study is to evaluate the effect of the happy aging education program on active aging determinants, and quality of life among community-based Muslim older adults compared with the control group who avail only health education.
Q1.• What is the effect of the BIHAAAP on physical, mental, and behavioral aspects of active aging among community-dwelling older adults in the compression to the control group who only avail health education? Q2. What is the effect of the BAAEP on the quality of life among community-dwelling older adults in Pakistan?
Treatment: (1) Face-to-face: 6 days, (2) home-based 12 weeks.
Comparison group: One-day orientation. After the trial, the control group availed of the booklet and video-recorded Muslim prayers-like exercises.
Full description
Road Map of the Study Development of BAAEP Development of content for face-to-face training consisted of lectures, group activities, and hand on practice with the intention to improve physical, mental, cognitive, and behavioral approaches for active aging.
Booklet contents: Tips on mindfulness eating habit practice to mentally prepare for any food items before eating, positive thought generation practice by different scenarios, benefits of exercises in pictorial form, pictures of healthy couples and beneficial effects of relationships, tips for spiritual health, and the booklet contents homework after each session.
Video development Detail about Muslim prayers like exercises
Study Area: Study setting: Two residential areas of Peshawar, Khyber Pakhtunkhwa
Sample selection process: Lady health workers (LHWs) will be approached through the District health office Peshawar and identified households with elders aged> 60 years from the family registration registers of each LHW.Identified 300 older adults in the jurisdiction of haji camp, skandertown, and Tarnab form.
Conduct a general health awareness program for all elders who registered with the five LHWs and will be given the responsibility of monitoring elders to perform exercises in their homes. A convenient sampling method will be used to recruit some of the elderly in the two regions of Peshawar in Khyber Pakhtunkhwa province.
Recruitment of the participant 2.1. Sample size calculation: Sample size will be calculated using G-power by priori power analysis. An effect size of 0.83 will be used from a previous study conducted on technology-based elder education. The sample size calculation will assume (i.e. α =0.05, power=0.8. Total 140.
2.2. Screening for eligibility: We will conduct a health awareness program in three high schools at different times in which around 300 elders participated. Arranged three points in which all elders were checked for cognitive, activity, auditory, and visual impairment levels.
2.2.1. Preliminary screening: screening will be conducted by physiotherapists and community health nurses for frailty, and severe health problems for example cardiac problems, cognitive problems auditory and severe visual problems (referred to psychologist, ENT specialist, and family medicines doctor.
2.2.2 Secondary screening: To register for trial the screening will be taken to take ( consent, registration, baseline assessment for sedentary lifestyles who reported spending less than 20 to 30 minutes per week outside in their home in the past month.
2.3. Sampling technique= Computer generated sequence will be employed to randomize study subjects either to intervention or control group and then a web-based data management system using a permuted block algorithm (with random block lengths) stratified by sex.
2.4. Treatment group=70, Control group=70 2.5. Treatment group= BAAEP, C= Usual activities Participants included: (a) sedentary retired adults aged 65 and older who reported spending less than 20 min per week in the past month
Procedure for implementation of treatment/ intervention 3.1. face: Three trainers(physiotherapist, community health nurse, psychologist) conducted the face-to-face sessions after getting training and piolet study. A PowerPoint presentation was prepared according to the protocol. piloting was done in the same setting to modify the discrepancies after taking feedback.
The setting was checked for ventilation, temperature, lighting, and chairs. 3.1.1. Setting for intervention: Three government high schools and one private high school were allocated for the training sessions by taking approval from the district education officer and the honor of a private school.
3.1.2. Three volunteers will be assigned for the setting and technical support through proper agreement. The generator was arranged for power backup during the session.
3.13.3. Interventions process: Orientation and three sections (1) didactic such as giving information and knowledge regarding aging, challenges and positive aspects of aging),(2) group activity for positive thinking, joke as an energizer, discussion on hobbies and interest,(3) hands-on training for( mind fullness and prayers like proper body movements exercises. Each group consisted of 15 participants, five-session in a day and each group availed 90 minutes sessions per week.
During the session continue feedback will be taken from the participants regarding any difficulty in performing exercises, understanding level, and further suggestions.
3.13.Transforming from face-to-face sessions to home-based training
Quality control: Homogeneous population characteristics; both male and female; data collectors and data analysts will be kept unaware of the research intention.
Participants were not blind due to the ethical considerations of the study. Researchers were not directly involved in the session and only observed the ongoing process, the researchers were not involved in the data collection process only randomly checking the objectivity, and researchers were not directly involved in data analysis to prevent biases. A person who will be unaware of the purpose of the study performed randomization of the total 140 elders in two groups. The research team was not aware of the outcome variables and was not involved in the data collection task. The data collectors were kept blind from the intervention strategies.
The study protocol is approved by the School of Nursing, Zhengzhou University. Written approval was taken from the School of Nursing, ZZU, and from the local health department of Khyber Pakhtunkhwa. Approval was taken from the local government of the province along with the readiness of the research teams and area representatives for conducting the session inside their premises of the area.
All participants were informed about the study and a written approval of willingness was taken from all the participants. In addition, their personal details are kept secret by assigning ID numbers and did not be used for any other purposes and this was well ensured.
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Inclusion Criteria:• Both males and females aged 60 or above
Exclusion Criteria:• Dependent older adults
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140 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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