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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04314921
Other study ID # LithuanianSportsU-3
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2018
Est. completion date September 30, 2019

Study information

Verified date March 2020
Source Lithuanian Sports University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Thirty-three healthy elderly people, who were classified into two age groups, participated in this study. All participants had not practiced yoga before and were asked not to perform any sports activities while the research was ongoing. In the experimental group, participants (n = 18) had to participate in 10 weeks of yoga classes. In the control group, participants (n = 15) did not perform any exercises or other changes in their daily living life.

Experimental measurements: Brunel, PSS-14 and HAD questionnaires


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date September 30, 2019
Est. primary completion date September 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years to 76 Years
Eligibility Inclusion Criteria:

- age, from 60 years old

- a statement by a local family physician about general good physical health

- never tired to practice yoga before

Exclusion Criteria:

- cardiovascular diseases

- musculoskeletal system diseases (osteoporosis, osteochondrosis, hernias)

- neurodegenerative diseases

- oncological diseases

- glaucoma

- injuries and surgeries in last 3 years

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Yoga trainings
10-week yoga sessions, 2 times per week, 90 min per session.

Locations

Country Name City State
Lithuania Lithuanian Sports Unviersity Kaunas

Sponsors (1)

Lead Sponsor Collaborator
Lithuanian Sports University

Country where clinical trial is conducted

Lithuania, 

Outcome

Type Measure Description Time frame Safety issue
Primary Brunel mood scale (BRUMS) The Lithuanian translated version of the Brunel Mood Scale (BRUMS) was used in the present study. It was based on the originally developed to serve as a brief measure of mood before and after yoga intervention. The BRUMS (1) scale has 24 items arranged into six subscales: anger, confusion, depression, fatigue, tension and vigor. Each subscale has a numerical rating scale (0 = not at all, 1 = a bit, 2 = moderate, 3 = enough; 4 = extremely) from which research participant select the one best represents at that time. The results within subscale is summed and a score range from 0 to 16 10 weeks
Primary Hospital anxiety and depression scale (HADS) To determine the level of anxiety and depression of subjects was used HADS scale. The scale consists of totally 14 questions with the answers valued from 0 to 3. Half of questions addressed to estimate anxiety and rest - depression. The total scoring and conclusion for the both categories of questions: 0-7 = Normal; 8-10 = Borderline abnormal (borderline case); 11-21 = Abnormal (case) 10 weeks
Primary Perceived stress scale -14 The purpose of this scale is to assess the degree of stress in subjects' lives. It consists of questions about the frequency of feeling and thoughts during the past time period. Potential answers: 0-never; 1-almost never; 2-sometimes; 3-fairly often and 4-very often. The scores are obtained by reversing the scores on the four positive items: for example, 0=4, 1=3, 2=2, etc. and then summing across all items. Scores for the 14-item form range from 0 to 56, with higher scores indicating greater perceived stress 10 weeks
Primary Human Free BDNF Venous blood samples from median antecubital vein were collected in 5 ml vacuum tubes with a gel separator and was separated by centrifugation (15 min at 1200g) to make blood serum. Samples were aliquoted and stored at -800C until analysis. The serum concentration of Human Free BDNF was measured using an enzyme-linked immunoassay kit (R&D Systems, Minneapolis, USA) 10 weeks
Primary Measurement of cognitive functions Automated Neuropsychological Assessment Metrics Version 4 (ANAM-4; Vista Life, USA) was used to measure neurocognitive skills: mental flexibility, verbal working memory, inhibition control, visuospatial processing. 10 weeks
Primary Psychomotor function evaluation Participants were assessed by Dynamic Parameter Analyzer (DPA-1). Its measure motor functions: accuracy, reaction speed-accuracy. 10 weeks
Primary Heart rate variability R-R intervals were recorded using a Polar H7 sensor with a chest strap (Kempele, Finland). 10 weeks
Primary Balance procedure Postural sway activity was measured by a posturography method with a single piezoelectric force plate (Kistler, Slimline System 9286, Switzerland). 10 weeks
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