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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04496778
Other study ID # P.T.REC/012/0027772
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 3, 2020
Est. completion date August 1, 2020

Study information

Verified date August 2020
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Alzheimer's is a type of dementia that affects memory, thinking and behavior. Symptoms eventually grow severe enough to interfere with daily tasks. this study aimed to delay the deterioration of anemic elderly condition as memory affection interfere with daily life activities and social interaction


Description:

Alzheimer's disease is the commonest cause of dementia and describes a clinical syndrome made up of three domains. First, a neuro-psychological domain encompassing those deficits of cognitive function such as amnesia (memory loss), aphasia (language disturbance), apraxia (the inability to carry out motor tasks despite intact motor functions) and agnosia (the inability to recognize people or objects despite intact sensory functions). Second, a group of psychiatric symptoms and behavioral disturbances, which have been termed neuro-psychiatric features, non-cognitive phenomena, or behavioral and psychological symptoms of dementia Alzheimer's disease is substantially increased among people aged 65 years or more, with a progressive decline in memory, thinking, language and learning capacity. Alzheimer's disease should be differentiated from normal age-related decline in cognitive function, which is more gradual and associated with less disability. Diabetes, hypertension, smoking, obesity, and dyslipidemia have all been found to increase risk as well a history of brain trauma, cerebrovascular disease, and vasculopathies.

Dementia affects approximately 5%-8% of individuals over age 65, 15%- 20% of individuals over age 75, and 25%-50% of individuals over age 85. Alzheimer disease is the most common dementia, accounting for 50%-75% of the total, with a greater proportion in the higher age ranges Dementia is expensive. The financial costs of managing Alzheimer's disease are enormous. The cost of illness is high in terms of both public and private resources. Families and caregivers who are required to provide care and patients affected by dementia also pay a high price in terms of their quality of life The primary goals of treatment are to maximize the patient's ability to function in daily life, maintain quality of life, slow the progression of symptoms, and treat depression or disruptive behaviors Low level laser therapy is a safe, non-invasive, and non-thermal modality that is based on a strong body of research dating back to the 1960.It involved in treating several conditions, the mechanisms of action involve the stimulation of mitochondria by the absorption of photons in cytochrome c oxidase, resulting in increased adenosine triphosphate production, reduced oxidative stress, anti-inflammatory effects, and increased focal cerebral blood flow


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date August 1, 2020
Est. primary completion date July 28, 2020
Accepts healthy volunteers No
Gender All
Age group 65 Years to 75 Years
Eligibility Inclusion Criteria:

- Sixty elderly patients aged from 65-75 y

- Body mass index (BMI) ranged from 30 to 34.9 kg/m2

- Mild cognitive dysfunction (Montreal cognitive assessment scores from 19-25

- Anemic

- The time between their diagnoses and participation in the study ranged from 6 months to 2 years

Exclusion Criteria:

- Moderate to severe cognitive impairment

- History of neurological disease ,stroke or Cardiovascular disease

- History of nasal bleeding or fracture

- Known photo-sensitivity disorder

- Current active cancer or within one year of cancer treatment or remission

- Serious mental health illness that in the opinion of the investigator would preclude the subject from study participation

- Active infection, wound or other external trauma to the target area to receive the laser therapy

- Participation in a clinical study or other type of research in the past 30 days

Study Design


Intervention

Device:
low level laser therapy ( laser acupuncture combined with nasal laser irradiation)
Cold Laser Therapy Watch (Laser Watch- 650 nm) combines acupuncture and nasal cavity for external blood irradiation. Laser watch with 10 laser beams - is applied to the left wrist. Nasal Probe with 2 laser beams - is applied to the nose cavity
Other:
aerobic exercise
3 d/week for 45 to 60 minutes per session for 3 months. started by 40%-50% Heart Rate Reserve (determined by using a walking treadmill exercise test) during the first 6 weeks increasing gradually up to 50%-70% Heart Rate Reserve

Locations

Country Name City State
Egypt Cairo Giza Dokki

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary change of cognitive function comparison of Montreal assessment scale scores before and after the intervention It range between 0 and 30. A score of 26 or over is considered to be normal. 3 months
Primary changes of hemoglobin level comparison of hemoglobin level for those anemic elderly before and after the intervention 3 months
Primary changes of balance comparison of berg balance scale scores before and after the intervention. It is a 14 item list with each item consisting of a five-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function 3 months
Primary changes of quality of life comparison of quality of life for Alzheimer disease scores before and after the intervention. It comprised of 13 items (physical health, energy, mood, living situation, memory, family, marriage, friends, self as a whole, ability to do chores, ability to do things for fun, money and life as a whole) for a total score of 13-52 with higher scores indicating better quality of life 3 months
Secondary changes of body mass index comparison of body weight (kilogram) before and after the study in relation to height per meter square (weight and height will be combined to report BMI in kg/m^2) 3 months
Secondary changes of waist hip ratio changes of waist hip ratio before and after the study 3 months
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