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Exercise Intervention for Employees of the University of Bern (WeMoveVirtual)

Primary Purpose

Neck Pain, Musculoskeletal Diseases, Occupational Health

Status
Completed
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Exercise intervention
Sponsored by
University of Bern
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neck Pain

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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).

Sites / Locations

  • University of Bern, Faculty of Human Sciences, Institute of Psychology

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Intervention

Arm Description

Exercise intervention

Outcomes

Primary Outcome Measures

Work performance
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

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

Full Information

First Posted
December 19, 2022
Last Updated
March 7, 2023
Sponsor
University of Bern
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1. Study Identification

Unique Protocol Identification Number
NCT05676528
Brief Title
Exercise Intervention for Employees of the University of Bern
Acronym
WeMoveVirtual
Official Title
Kurzbewegungsintervention für Mitarbeitende Der Universität Bern
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
October 1, 2022 (Actual)
Primary Completion Date
January 31, 2023 (Actual)
Study Completion Date
January 31, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Bern

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neck Pain, Musculoskeletal Diseases, Occupational Health, Efficiency, Exercise Therapy, Work Performance, Presenteeism

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Exercise intervention
Intervention Type
Other
Intervention Name(s)
Exercise intervention
Intervention Description
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.
Primary Outcome Measure Information:
Title
Work performance
Description
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).
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Intensity of neck pain
Description
Change in neck pain from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means worse.
Time Frame
Over the period of 6 weeks
Title
Intensity of back pain
Description
Change in back pain from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means worse.
Time Frame
Over the period of 6 weeks
Other Pre-specified Outcome Measures:
Title
Level of physical activity
Description
Change of the level of physical activity from baseline. Questionnaire, single item (yes / no).
Time Frame
Over the period of 6 weeks
Title
Sleep quality
Description
Change in sleep quality from baseline. Numeric Rating scale. Min = 1, Max = 5. Higher score means worse.
Time Frame
Over the period of 6 weeks
Title
Work breaks
Description
Change in work breaks from baseline. Questionnaire, single item (number of work breaks)
Time Frame
Over the period of 6 weeks
Title
General health status
Description
Change in general health status from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means better.
Time Frame
Over the period of 6 weeks
Title
Mental health status
Description
Change in mental health status from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means better.
Time Frame
Over the period of 6 weeks
Title
Flexibility
Description
Change in self-rated flexibility of the muscles from baseline. Numeric Rating Scale. Min = 0, Max = 10. Higher score means better.
Time Frame
Over the period of 6 weeks
Title
Adherence to exercise 1
Description
Number of exercise from baseline. Via PhysiApp. Higher score means higher number of exercise.
Time Frame
Over the period of 6 weeks
Title
Adherence to exercise 2
Description
Type of exercise from baseline. Via PhysiApp. Strengthening vs. non-strengthening.
Time Frame
Over the period of 6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Achim Elfering, Prof
Organizational Affiliation
University of Bern
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Bern, Faculty of Human Sciences, Institute of Psychology
City
Bern
ZIP/Postal Code
3012
Country
Switzerland

12. IPD Sharing Statement

Plan to Share IPD
No

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Exercise Intervention for Employees of the University of Bern

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