Aging Disorder, Disability Physical, Pain
Conditions
Keywords
Therapeutic exercise,, manual therapy,, elderly,, geriatrics,, pain,, disability.
Brief summary
This research project is part of the process of generating scientific evidence, on whether the clinical results obtained, in the treatment of the consequences of aging on mobility, pain and disability, are better if therapeutic exercise programs are added sessions of manual therapy and training in pain awareness, or on the contrary, do not significantly modify the effect of exercise programs.
Detailed description
General objective: Find out if adding Manual Therapy (MT) sessions to therapeutic exercise programs increases the efficacy of clinical results for the treatment of ailments derived from aging in older adults (65 \<age \<85). Specific objectives: 1. Assess the effects on pain. (hypothesis: MT improves pain outcomes) 2. Assess the effects on physical disability. (hypothesis: MT improves results regarding physical disability) 3. Assess the effects on mental disability. (hypothesis: MT improves results regarding mental disability) 4. Assess the effects on the prevention of falls (hypothesis: MT improves the results regarding the risk of falls) Methodology: Study design: It is a study of the randomized clinical trial type, with triple blind. Selection of participants: 1\. General criteria: * The sample will be selected from the patients who volunteer to participate in the study, which will be announced by the media (Radio and / or TV) and meet the inclusion criteria and not the exclusion criteria. * Participants will be treated by different therapists, who will be instructed in the treatments to be performed on the participants, to eliminate the therapist's personal factor as a contaminating variable. * Participants will be referred to the physiotherapist according to the group assigned by the randomization process, which will be unknown by the patient. Sample size: To calculate the sample size, the EPIDAT 4.2 or GRANMO 7.12 computer program will be used, depending on the population and epidemiological data of the Catalunya area, of older adults, with disabilities and mechanical-degenerative pain. If the calculation is made based on a Student's t test for independent data, accepting an alpha risk of 0.05 and a beta risk of 0.20 in a bilateral contrast, 25 subjects would be required in each group to detect a minimum difference of 20 percentage points. between two groups, assuming a common standard deviation of 25 points, and a loss to follow-up rate of 0%, following the usual criteria of biostatistics in health sciences (1) and the criteria of minimal differences between groups previously used in similar pilot studies. In case of loss of subjects in the sample, participants should be replaced by others to maintain proportions. The definitive calculations will be made with more precision after the epidemiological study mentioned above. Randomization Of all the participants who meet the inclusion criteria and do not have any exclusion criteria, a number will be assigned, after being randomized through a computerized process, to distribute each number to the corresponding group. The patient will not know which group he has been assigned to. Analytical procedure: Analysis by computer processing with SPSS 22.0 ® program. Performed by a blinded computer analyst. Ethical aspects: During the study, national and international guidelines (code of ethics, Declaration of Helsinki) will be followed, as well as the legal regulations on data confidentiality (Organic Law 3/2018 of December 5 on the Protection of Personal Data and guarantee of digital rights -LOPD-).
Interventions
OTHERExercise
Exercises for body mobility and muscle toning, Sophrology
OTHERManual Therapy
Exercises for body mobility and muscle toning, Sophrology, musculoskeletal oscillatory manual therapy
Sponsors
Omphis Foundation
Juan Vicente, López Díaz
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Masking description
A triple blinding will be carried out: 1) of the patient, 2) of the collaborator who performs the data collection, 3) of the computer data analyst. The physiotherapist who performs the intervention of manual therapy, exercise teaching and pain education, it is impossible to blind him.
Intervention model description
It is a study of the randomized clinical trial
Eligibility
Sex/Gender
ALL
Age
65 Years to 85 Years
Healthy volunteers
Yes
Inclusion criteria
* People of both sexes. * Between 65 and 85 years of age. * No acute pathologies at the time of selection. * Who present symptoms of muscle-joint degenerative mechanical aging with an intensity score greater than 4 on a scale of 0-10.
Exclusion criteria
* Patients with a recent traumatic history. * Presence of an acute-type radiation component of neurological origin to upper or lower limbs. * With neurological alterations both central and peripheral. * Who are taking opioid-based analgesic medication, gabapentin, etc. * Patients with severe malformations. * Who are following any other type of treatment, be it manual or physical agents or alternative or complementary therapies. * Those who have been treated with infiltrations or the like in a period of less than a year before starting the study. * Patients with a serious psychiatric history such as schizophrenia or psychopathies. * Patients with cognitive impairment. * Patients with vestibular problems that cannot tolerate oscillatory movements. * Those who are contraindicated due to their general metabolic or cardiopulmonary state to carry out moderate physical exercise.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change of subjective assessment of pain intensity | beginning and through study completion, an average of 12 weeks | using a VAS TEST (Visual Analog Score for pain) (Minimum = 0 better and maximum = 10 worse) |
| Change of the qualitative aspects of pain | beginning and through study completion, an average of 12 weeks | using the McGill pain questionnary |
| Change of of disability and health status | beginning and through study completion, an average of 12 weeks | using the SF36 test (36-item short form health survey) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change of risk of falls | beginning and through study completion, an average of 12 weeks | Tinetti test. (test for balance and gait) (Minimum = 0 worse and maximum = 28 better) |
| Change of Physical activity in older adults | beginning and through study completion, an average of 12 weeks | PASE test (Physical Activity Scale for the Elderly) |
Outcome results
None listed