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Minimum dose of intervention duration with effect on trunk stability and compensation of perturbations conducted within the MiSpEx-Network [National Research Network for Medicine in Spine Exercise]: National research network for diagnosis, prevention and treatment of back pain for elite athletes and the general population

Minimum dose of intervention duration with effect on trunk stability and compensation of perturbations conducted within the MiSpEx-Network [National Research Network for Medicine in Spine Exercise]: National research network for diagnosis, prevention and treatment of back pain for elite athletes and the general population - MiSpEx - Intervention Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00012917
Enrollment
80
Registered
2017-08-22
Start date
2017-09-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

healthy participants M54

Interventions

Group 1: Control Group: core-specific sensorimotor training with additional perturbation with 6 sessions in 3 weeks (4 exercises, 3 sets á 10 repetitions
home-based) Group 2: Intervention group I: core-specific sensorimotor training with additional perturbation with 6 sessions in 3 weeks (3 exercises, 2 sets á 10 repetitions
home-based) Group 3: Intervention group II: core-specific sensorimotor training with additional perturbation with 6 sessions in 3 weeks (2 exercises, 2 sets á 10 repetitions
home-based) Group 4: Intervention group III: core-specific sensorimotor training with additional perturbation with 6 sessions in 3 weeks (1 exercise, 3 sets á 10 repetitions
home-based)

Sponsors

Hochschulambulanz der Universität Potsdam
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: both gender; aged 18 - 50 years

Exclusion criteria

Exclusion criteria: Acute infection, pregnancy, any illness that contraindicates exercise, as well as acute or chronic back pain

Design outcomes

Primary

MeasureTime frame
trunk strength: isokinetic maximum strength capacity [Nm] with and without additional perturbation is assessed pre and post intervention period (M1/M2) by use of dynamometers.

Secondary

MeasureTime frame
neuromuscular adaptation for perturbations: assessment by the muscular activity (EMG: time/amplitude measures). Before and after 3 weeks intervention.

Countries

Germany

Contacts

Public ContactJosefine Stoll

Hochschulambulanz der Universität Potsdam

sportmedizin@uni-potsdam.de00493319771125

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 5, 2026