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Exercise Intervention for Employees of the University of Bern

Kurzbewegungsintervention für Mitarbeitende Der Universität Bern

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05676528
Acronym
WeMoveVirtual
Enrollment
24
Registered
2023-01-09
Start date
2022-10-01
Completion date
2023-01-31
Last updated
2023-03-08

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

Conditions

Efficiency, Exercise Therapy, Musculoskeletal Diseases, Neck Pain, Occupational Health, Presenteeism, Work Performance

Brief summary

As part of a Swiss National Science Foundation SNSF project (On-site multi-component intervention to improve productivity and reduce the economic and personal burden of neck pain in Swiss Office-Workers, NEXpro = Neck EXercises for productivity, SNSF no. 32003B\_182389, BASEC no. 2019-01678), the investigators first developed a physiotherapeutic exercise intervention to improve the strength and mobility of the neck muscles. In the SNSF project NEXpro, the intervention took place on-site in the office. However, in view of the digital transformation, it is important to adapt the intervention delivery method to the new virtual work setting. The aims of the present project are therefore to implement, further develop and contextually adapt the exercise intervention in order to reduce musculoskeletal complaints and to reduce health-related presenteeism. The final product is a user-friendly virtual 6-week short exercise intervention that employees of the University of Bern can use independently, regardless of time and place. The effectiveness of the newly developed short exercise intervention (pain reduction, reduction of presenteeism) will be assessed during a short pilot phase.

Interventions

OTHERExercise intervention

The participants will carry out a physiotherapeutic exercise intervention over a period of 6 weeks. The exercise intervention is stored in a smartphone app (PhysiApp) and consists of different neck and shoulder exercises. The investigators will provide the training material to the participants and they may keep it after the end of the study. Participants can choose which and how many exercises they would like to do. However, the investigators ask participants to exercise at least three times a week for 20 minutes each time (a total of one hour per week) and to document the training afterwards in the smartphone app. In the first, third and sixth week, the investigators train together with the participants via a virtual platform (e.g. video call via Microsoft Teams) so that the correct execution of the exercise can be checked and questions can be clarified.

Sponsors

University of Bern
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Employees of the Faculty of Human Sciences of the University of Bern who * suffer from neck pain or would like to prevent neck pain * are between 18 and 65 years of age * understand German (written and oral) * have a predominantly sedentary job * have given written consent to participate in the study. Note: Neither gender, age, education nor group affiliation play a role. The investigators particularly welcome participation from mid-level employees. If students are willing to participate, they may also do so, but this group will not be actively recruited.

Exclusion criteria

* Existing severe neck pain grade IV (neck trauma, neck injury, specific pathologies (e.g. congenital cervical anomalies, stenosis, radiculopathy), inflammatory conditions (e.g. rheumatoid arthritis), history of cervical surgery) * If physical activity is contraindicated by the doctor for any reason (e.g. due to unresolved hypertension).

Design outcomes

Primary

MeasureTime frameDescription
Work performance6 weeksChange in work performance from baseline. Work Productivity and Activity Impairment Questionnaire (i.e., work productivity loss). Min = 0, Max = 100. Higher score means worse (higher work productivity loss).

Secondary

MeasureTime frameDescription
Intensity of neck painOver the period of 6 weeksChange in neck pain from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means worse.
Intensity of back painOver the period of 6 weeksChange in back pain from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means worse.

Other

MeasureTime frameDescription
General health statusOver the period of 6 weeksChange in general health status from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means better.
Mental health statusOver the period of 6 weeksChange in mental health status from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means better.
Level of physical activityOver the period of 6 weeksChange of the level of physical activity from baseline. Questionnaire, single item (yes / no).
Adherence to exercise 1Over the period of 6 weeksNumber of exercise from baseline. Via PhysiApp. Higher score means higher number of exercise.
Adherence to exercise 2Over the period of 6 weeksType of exercise from baseline. Via PhysiApp. Strengthening vs. non-strengthening.
FlexibilityOver the period of 6 weeksChange in self-rated flexibility of the muscles from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means better.
Sleep qualityOver the period of 6 weeksChange in sleep quality from baseline. Numeric Rating scale. Min = 1, Max = 5. Higher score means worse.
Work breaksOver the period of 6 weeksChange in work breaks from baseline. Questionnaire, single item (number of work breaks)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026