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Gamified Rehab vs Take-home Packet Rehab for Non-specific Low Back Pain

The Effects of a Gamified Rehabilitation Protocol Compared to an At-Home Exercise Packet in Individuals With Low Back Pain

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05573932
Enrollment
40
Registered
2022-10-10
Start date
2022-10-13
Completion date
2025-06-30
Last updated
2023-11-28

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

Conditions

Non-specific Low Back Pain

Brief summary

Two groups with non-specific low back pain will be completing the same exercise protocol. The leaderboard group will have a gamified experience and the take-home packet group will be using a paper take-home packet. Outcomes will be measured at 3 weeks, 6 weeks, with pain and disability also being measured at 12 and 18 months.

Detailed description

There will be two groups in this study, the leaderboard group, and the take-home packet group. The leaderboard group and the take-home packet group will be completing the same exercise program throughout the 6-weeks. The exercises included the plank, side plank (left and right side), foot elevated (left and right side), dead bug and bird dog exercise until discontinuation. The exercises will increase with repetitions every two weeks and that outline is listed below in procedures involved. The leaderboard group will have on demand video access to the exercises and the take-home packet group will have a take-home packet. The leaderboard group will also be receiving weekly leaderboards of average and top exercise durations of the leaderboard group participants. The audio description of exercise in the on-demand video group is the same script as the written description in the take-home packet.

Interventions

OTHERLeaderboard

De-identified leaderboard showing average durations of exercises completed by all participants in leaderboard group.

OTHERTake-home packet

Take-home packet of exercises.

Sponsors

University of Central Florida
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Participants will be randomized into the two separate groups using a random number generator and allocation will be concealed in opaque envelopes prior to data collection.

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Must be 18-45 years old * Biological sex of Male or Female * Self-reported low back pain within the previous 6 months or greater than 3 episodes within the past 3 years

Exclusion criteria

* Must not be currently seeing and or receiving care from an athletic trainer, physical therapist, or other rehabilitation specialist in the previous 6 months * Must not have low back pain conditions such as lumbar spondylosis, herniated disc, spondylolisthesis, previous spine surgery, currently pregnant, experiencing neurological symptoms or other muscular abnormalities * Unable to assume the exercise starting position * Current use of lidocaine patches or prescription pain medicine

Design outcomes

Primary

MeasureTime frameDescription
AdherenceChange from baseline to 3 weeksAssessed by the exercise adherence rating scale
Change in painChange from baseline to 3 weeksAssessed by the numeric pain rating scale
Change in DisabilityChange from baseline to 3 weeksAssessed with the Oswestry Disability Index
Change in Muscle thickness of the lateral abdominal wallChange from baseline to 6 weeksAssessed with ultrasound during static positions and exercise starting positions

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026