NCT06321926

Brief Summary

The goal of this study (waitlist control study) is to evaluate the effectiveness of the ActiveWaiting App on increasing physical activity and improving quality of life in physically inactive adults in Austria. The main questions it aims to answer are:

  • on physical activity behaviour and
  • on quality of life.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
33

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2024

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 27, 2024

Completed
22 days until next milestone

First Posted

Study publicly available on registry

March 20, 2024

Completed
12 days until next milestone

Study Start

First participant enrolled

April 1, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 24, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 24, 2024

Completed
Last Updated

June 25, 2024

Status Verified

June 1, 2024

Enrollment Period

3 months

First QC Date

February 27, 2024

Last Update Submit

June 24, 2024

Conditions

Keywords

sedentary behaviourbehaviour changedigital health

Outcome Measures

Primary Outcomes (2)

  • Amount of physical activity in minutes per day

    Participants are asked to report their physical activity twice a day (noon and evening).

    up to 2 weeks

  • EQ VAS / EQ-5D-5L

    The EQ VAS (EuroQol Visual Analog Scale) is the last item in the EQ-5D-5L (EuroQol - 5 Dimension - 5 Level) Questionnaire. It records the respondent's overall current health on a visual analogue scale. The endpoints are labelled as 'The best health you can imagine' (=100) and 'The worst health you can imagine' (=0). The EQ VAS provides a quantitative measure of the person's perception of their overall health and is used in this study.

    up to 2 weeks

Secondary Outcomes (2)

  • App usage - exercise session length

    7 days

  • App usage - total duration per session

    7 days

Study Arms (2)

Intervention group

EXPERIMENTAL

Participants in the intervention group use the ActiveWaiting App for one week.

Device: ActiveWaiting App

Waitlist control group

OTHER

Participants in the waitlist control group go through a one-week control period without any intervention first, before they are using the app for one week.

Device: ActiveWaiting App

Interventions

The final prototype aims at increasing physical activity during the day by providing exercises for waiting periods and other idle time periods. The user can choose from a pool of exercises from five different categories (11 exercises for endurance, 65 exercises for strength, 67 exercises for flexibility, 11 exercises for relaxation, or 5 exercises for balance). Additionally, within each category, the user can choose only "discrete" exercises which are not noticeable to an observer. If the user has used the app before, the last or previously saved settings can be chosen. Every input field has an information icon showing a short description of the input field.

Intervention groupWaitlist control group

Eligibility Criteria

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

You may qualify if:

  • a sedentary lifestyle (expressed in a full to part-time sedentary job)
  • using a smart phone seven days a week
  • ability to operate an app on the smart phone
  • age between 18 and 65 years

You may not qualify if:

  • prior usage of the ActiveWaiting App
  • achieving the World Health Organization (WHO) recommendations for physical activity (assessed via Rapid Assessment of physical Activity RAPA)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

FH Campus Wien

Vienna, Austria

Location

MeSH Terms

Conditions

Sedentary Behavior

Condition Hierarchy (Ancestors)

Behavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
CARE PROVIDER, OUTCOMES ASSESSOR
Masking Details
Outcomes will be selected via lime survey. Allocation to the groups will be concealed.
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Participants are assigned to the intervention group or the waitlist control group. The intervention group uses the ActiveWaiting App for a week, the waitlist control group starts with a control period (one week), before using the App for a week.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 27, 2024

First Posted

March 20, 2024

Study Start

April 1, 2024

Primary Completion

June 24, 2024

Study Completion

June 24, 2024

Last Updated

June 25, 2024

Record last verified: 2024-06

Data Sharing

IPD Sharing
Will not share

Locations