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Real-time Videoconference-based Exercise in Eldercare Workers

Effects of a Real-time Videoconference-based Exercise Program in Eldercare Workers: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05050526
Acronym
ReViEEW
Enrollment
130
Registered
2021-09-20
Start date
2021-10-01
Completion date
2024-04-30
Last updated
2024-05-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Disorders, Pain

Keywords

Eldercare, Caregiver, Exercise, Tele-health, Musculoskeletal disorders, Mental disorders, Absenteeism, Work ability, Work performance

Brief summary

Formal caregiving of elderly dependent people is a both physically and psychologically demanding job, and both musculoskeletal and mental disorders with a negative impact in general health and quality of life are habitual among eldercare workers. Previous research has shown that physical exercise programs can reduce and/or prevent those disorders, consequently improving well-being at work. Online exercise interventions might be a cost-effective tool, as they can reach a large number of people at a relatively low cost. Moreover, they are compatible with situations in which interpersonal physical distancing is required, such as the current COVID-19 pandemic. However, real-time videoconference-based exercise interventions have not yet been studied in working populations. Thus, the aim of this study is to assess the effects of a real-time videoconference-based exercise intervention in eldercare workers. The primary outcome will be low back pain. Pain in neck, shoulders and wrists/hands will also be recorded, as well as additional measures of physical fitness, psychoaffective state, health and work-related variables. All outcomes will be measured at baseline and at 12-week and 48-week follow-ups.

Interventions

BEHAVIORALReal-time videoconference-based Exercise program

12-week exercise program consisting of two weekly 45 minute group-based sessions, remotely supervised by a professional via real-time videoconference. Each session will consist of a warm-up (5-10 min), general strengthening (30 min) and cool-down (5-10 min). Warm-up will include general joint mobility and exercises focused on increasing heart rate. General strengthening will include 4 series of 6 exercises (2 for lower limb, 2 for upper limb and 2 for the trunk) performed with minimal equipment, combining body-weight and elastic-band exercises. Three difficulty levels will be set for each of the exercises, and progression will be made at weeks 5 and 9. Participants will be asked to work in a given rate of perceived exertion (between 3 and 5 in Borg's CR10 scale) and not to reach failure in any of the exercises. Cool-down will include stretching and breathing/relaxing exercises.

Sponsors

Caser Residencial Betharram
CollaboratorUNKNOWN
Fundación Aspaldiko
CollaboratorUNKNOWN
Grupo Servicios Sociales Integrados
CollaboratorUNKNOWN
Igurco Residencias Sociosanitarias
CollaboratorUNKNOWN
Grupo Colisée
CollaboratorUNKNOWN
Ander Espin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

The investigators in charge of doing the statistical analysis and assessing the outcome measures (e.g., physical performance tests) will be blinded to group allocation. Due to the characteristics of the study, blinding of the participants (i.e., eldercare workers) and the care provider (i.e., professional conducting the exercise sessions) to the group allocation is not possible.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Professional eldercare workers with ≥3 months of experience in the profession * Employment contract at least until the anticipated date of study end

Exclusion criteria

* Pregnancy * Contraindication to exercise according to the American College of Sports Medicine Guidelines

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline average pain intensity at 12 weeksAt baseline and at 12-week follow-upAverage pain intensity during the last 7 days in a Numerical Rating Scale for pain ranging from 0 (complete absence of pain) to 10 (worst imaginable pain). This information will be collected for pain in the low back, neck, shoulders and wrists/hands.
Change from baseline average pain intensity at 48 weeksAt baseline and at 48-week follow-upAverage pain intensity during the last 7 days in a Numerical Rating Scale for pain ranging from 0 (complete absence of pain) to 10 (worst imaginable pain). This information will be collected for pain in the low back, neck, shoulders and wrists/hands.
Change from baseline highest pain intensity at 12 weeksAt baseline and at 12-week follow-upHighest pain intensity during the last 7 days in a Numerical Rating Scale for pain ranging from 0 (complete absence of pain) to 10 (worst imaginable pain). This information will be collected for pain in the low back, neck, shoulders and wrists/hands.
Change from baseline highest pain intensity at 48 weeksAt baseline and at 48-week follow-upHighest pain intensity during the last 7 days in a Numerical Rating Scale for pain ranging from 0 (complete absence of pain) to 10 (worst imaginable pain). This information will be collected for pain in the low back, neck, shoulders and wrists/hands.
Change from baseline pain frequency at 12 weeksAt baseline and at 12-week follow-upNumber of days in pain during the last 7 days (0-7). This information will be collected for pain in the low back, neck, shoulders and wrists/hands.
Change from baseline pain frequency at 48 weeksAt baseline and at 48-week follow-upNumber of days in pain during the last 7 days (0-7). This information will be collected for pain in the low back, neck, shoulders and wrists/hands.
Change from baseline pain interference at 12 weeksAt baseline and at 12-week follow-upNumber of days in which pain negatively interferes with work during the last 7 days of work (0-7). This information will be collected for pain in the low back, neck, shoulders and wrists/hands.
Change from baseline pain interference at 48 weeksAt baseline and at 48-week follow-upNumber of days in which pain negatively interferes with work during the last 7 days of work (0-7). This information will be collected for pain in the low back, neck, shoulders and wrists/hands.

Secondary

MeasureTime frameDescription
Hypnotic/anxiolytic medication consumption frequencyAt baseline and at 12-week and 48-week follow-upsNumber of days in which hypnotic/anxiolytic medication is taken during the last 7 days (0-7).
EuroQol-5D 0-100 health state scaleAt baseline and at 12-week and 48-week follow-upsIt measures self-perceived current health state in a scale ranging from 0 (worst imaginable health state) to 100 (best imaginable health state).
Work AbilityAt baseline and at 12-week and 48-week follow-upsWork ability will be assessed by the following item extracted from the Workability Index: assuming that your work ability at its best has a value of 10 points, how many points would you rate your current work ability?. Participants are asked to give a score ranging from 0 (completely unable to work) to 10 (lifetime best work ability).
Kneeling push-up testAt baseline and at 12-week and 48-week follow-upsIt measures upper limb strength based on the maximum number of knee push-ups the participant can perform until failure.
Borg's CR-10 scale for perceived physical exertion at workAt baseline and at 12-week and 48-week follow-upsIt measures perceived physical exertion while doing physical work in a scale ranging from 0 (nothing at all) to 10 (extremely strong).
AbsenteeismAt baseline and at 12-week and 48-week follow-upsDays of absence from work during the last year will be collected from the official registry of the company and by self-reported questionnaire. Presence of absenteeism (yes/no), days of absence (n) and reason will be collected.
Work PerformanceAt baseline and at 12-week and 48-week follow-upsWork performance will be assessed by the following item extracted from the World Health Organization Health and Work Performance Questionnaire: On a scale from 0 to 10 where 0 is the worst job performance anyone could have at your job and 10 is the performance of a top worker, how would you rate your overall work performance on the days you worked during the last 12 weeks? Participants are asked to give a score between 0 and 10.
Analgesic medication consumption frequencyAt baseline and at 12-week and 48-week follow-upsNumber of days in which analgesic medication is taken during the last 7 days (0-7).
5-repetition sit-to-stand testAt baseline and at 12-week and 48-week follow-upsIt measures lower limb strength based on the time taken by the participant to get up from and sit down on a chair five times as quickly as possible.
Shirado-Ito trunk flexor endurance testAt baseline and at 12-week and 48-week follow-upsIt measures trunk flexor endurance based on the maximum time the participant is able to maintain a defined body position, which mainly activates trunk flexor muscles.
Subjective Happiness scaleAt baseline and at 12-week and 48-week follow-upsIt is comprised of 4 items, each of them answered with a score between 1 and 7. A single composite score is obtained by averaging the responses to the 4 items, and a higher score corresponds to a greater happiness.
Goldberg Anxiety and Depression scaleAt baseline and at 12-week and 48-week follow-upsThe scale includes 9 items for anxiety symptoms and 9 items for depression symptoms. Each item is answered with a Yes or a No. A higher number of positive answers corresponds to a higher risk of suffering a clinically relevant anxiety or depression disorder, respectively.
Maslach Burnout InventoryAt baseline and at 12-week and 48-week follow-upsThe Inventory is comprised of 22 items corresponding to three domains: personal accomplishment, emotional exhaustion and depersonalization. Each item is answered in a 0-6 Likert scale depending on the frequency with which the participant experiences the feelings described. One total score per domain is obtained.
Single-Item Sleep Quality ScaleAt baseline and at 12-week and 48-week follow-upsIt evaluates overall sleep quality in the last 7 days with a numerical scale that ranges between 0 (terrible) and 10 (excellent).

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 9, 2026