WeMoveVirtual: Exercise Intervention for Employees of the University of Bern

Sponsor
University of Bern (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05676528
Collaborator
(none)
24
1
1
3
8

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Exercise intervention
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
24 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Kurzbewegungsintervention für Mitarbeitende Der Universität Bern
Actual Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Exercise intervention

Other: Exercise 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.

Outcome Measures

Primary Outcome Measures

  1. Work performance [6 weeks]

    Change 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 Outcome Measures

  1. Intensity of neck pain [Over the period of 6 weeks]

    Change in neck pain from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means worse.

  2. Intensity of back pain [Over the period of 6 weeks]

    Change in back pain from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means worse.

Other Outcome Measures

  1. Level of physical activity [Over the period of 6 weeks]

    Change of the level of physical activity from baseline. Questionnaire, single item (yes / no).

  2. Sleep quality [Over the period of 6 weeks]

    Change in sleep quality from baseline. Numeric Rating scale. Min = 1, Max = 5. Higher score means worse.

  3. Work breaks [Over the period of 6 weeks]

    Change in work breaks from baseline. Questionnaire, single item (number of work breaks)

  4. General health status [Over the period of 6 weeks]

    Change in general health status from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means better.

  5. Mental health status [Over the period of 6 weeks]

    Change in mental health status from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means better.

  6. Flexibility [Over the period of 6 weeks]

    Change in self-rated flexibility of the muscles from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means better.

  7. Adherence to exercise 1 [Over the period of 6 weeks]

    Number of exercise from baseline. Via PhysiApp. Higher score means higher number of exercise.

  8. Adherence to exercise 2 [Over the period of 6 weeks]

    Type of exercise from baseline. Via PhysiApp. Strengthening vs. non-strengthening.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts 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).

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Bern, Faculty of Human Sciences, Institute of Psychology Bern Switzerland 3012

Sponsors and Collaborators

  • University of Bern

Investigators

  • Principal Investigator: Achim Elfering, Prof, University of Bern

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Bern
ClinicalTrials.gov Identifier:
NCT05676528
Other Study ID Numbers:
  • 2022-08-01
  • 2022-00970
First Posted:
Jan 9, 2023
Last Update Posted:
Jan 9, 2023
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 9, 2023