NCT05676528

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Oct 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2022

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

December 19, 2022

Completed
21 days until next milestone

First Posted

Study publicly available on registry

January 9, 2023

Completed
22 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2023

Completed
Last Updated

March 8, 2023

Status Verified

March 1, 2023

Enrollment Period

4 months

First QC Date

December 19, 2022

Last Update Submit

March 7, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • 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).

    6 weeks

Secondary Outcomes (2)

  • Intensity of neck pain

    Over the period of 6 weeks

  • Intensity of back pain

    Over the period of 6 weeks

Other Outcomes (8)

  • Level of physical activity

    Over the period of 6 weeks

  • Sleep quality

    Over the period of 6 weeks

  • Work breaks

    Over the period of 6 weeks

  • +5 more other outcomes

Study Arms (1)

Intervention

EXPERIMENTAL

Exercise intervention

Other: Exercise intervention

Interventions

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.

Intervention

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

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

Bern, 3012, Switzerland

Location

MeSH Terms

Conditions

Neck PainMusculoskeletal Diseases

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Achim Elfering, Prof

    University of Bern

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 19, 2022

First Posted

January 9, 2023

Study Start

October 1, 2022

Primary Completion

January 31, 2023

Study Completion

January 31, 2023

Last Updated

March 8, 2023

Record last verified: 2023-03

Data Sharing

IPD Sharing
Will not share

Locations