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Validation of Electronic Visual Analogue Scales (VAS) for Subjective Measures in older adults in rehabilitation for musculoskeletal and neurological conditions; Pain, Fatigue, Exertion, Enjoyment and Perceived benefits

A comparison of the use of visual analogue scales using paper based and iPad based VAS for Pain, Fatigue, Exertion, Enjoyment and Perceived benefits in older adults in rehabilitation

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000283572
Enrollment
22
Registered
2015-03-25
Start date
2014-12-01
Completion date
2015-05-07
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The aim of this study is determine if data collected on a mobile device has the same accuracy and reliability as the traditional paper based method of data collection. Data collection using mobile technology (including iPads) has the capacity to improve the efficiency of data collection and reduce transcription errors in large data sets. Measurement of subjective measures such as Pain, Fatigue, Exertion, Enjoyment and Perceived benefits of an intervention allow researchers to determine valuable information, from the perspective of the participants, in any intervention that they are carrying out. These factors have been identified as important barriers or facilitators to participation in in physical activity or exercise programs. Tools to measure these parameters have been validated in paper form. In larger studies the ability to collect this data electronically has huge potential to improve research efficiency, but to date no validation studies have been done using the iPad and these tools in an older population. Advantages: *Reduced time for data collection *Improved storage of data (no paper copies required) *Reduced research time (no data transcription required) *Easy ability to securely gain and store de-identified/re-identifiable data

Interventions

Data will be collected once using a touch screen on an iPad device. Participants wil complete 4 screens using their finger on a touch screen and complete a VAS Pain, VAS fatigue, borg rating of exertion, plus a rating scale for enjoyment, perceived benefit and ease of use. It is anticipated that it would take 5 minutes to explain and complete

Sponsors

The University of Tasmania
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Diagnosis
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Older adults attending for exercise class or rehabilitation for musculoskeletal or neurological conditions

Exclusion criteria

Neurological conditions that impact on communication and prohibit informed consent to be made including aphasia dementia cognitive impairment vision

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026