search
Back to results

Telehealth Support to Increase Physical Activity in Rett Syndrome (ActivRett)

Primary Purpose

Rett Syndrome

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Telehealth-delivered participation strategies to increase physical activity
Sponsored by
Telethon Kids Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rett Syndrome focused on measuring Sedentary behaviour, Physical activity, Quality of life, Telehealth

Eligibility Criteria

5 Years - 40 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Genetically confirmed Rett syndrome
  • Able to stand (with or without assistance)
  • Live in Australia, Denmark or Israel

Exclusion Criteria:

  • Individuals who have had spinal fusion over the previous 12 months
  • Individuals who have had lower extremity orthopaedic surgery over the previous 6 months

Sites / Locations

  • Center for Rett Syndrom, RigshospitaletRecruiting
  • Ari'el UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Waitlist-Control Group

Immediate Treatment

Arm Description

The 'waitlist control' group will receive the 12-week non-intervention period first, followed by 12 week intervention period.

The 'immediate treatment' group will receive the 12-week intervention period first, followed by 12 week non-intervention period.

Outcomes

Primary Outcome Measures

Average daily uptime (%)
Percentage of time spent active (uptime) over total awake time, measured with an ActivPAL
Average daily step count
Number of daily steps measured by Stepwatch Activity Monitor

Secondary Outcome Measures

Sleep quality
Sleep Disturbance Scale for Children.
Behaviour
Rett Syndrome Behaviour Scale
Child Quality of Life
Quality of Life Inventory-Disability (QI-Disability)

Full Information

First Posted
November 14, 2019
Last Updated
February 2, 2020
Sponsor
Telethon Kids Institute
Collaborators
Rigshospitalet, Denmark, Ariel University, University of Haifa
search

1. Study Identification

Unique Protocol Identification Number
NCT04167059
Brief Title
Telehealth Support to Increase Physical Activity in Rett Syndrome
Acronym
ActivRett
Official Title
Implementing Telehealth Support to Increase Physical Activity in Girls and Women With Rett Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2020 (Actual)
Primary Completion Date
September 1, 2020 (Anticipated)
Study Completion Date
September 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Telethon Kids Institute
Collaborators
Rigshospitalet, Denmark, Ariel University, University of Haifa

4. Oversight

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

5. Study Description

Brief Summary
This study will recruit families with a daughter with Rett syndrome living in either Australia, Denmark or Israel, and thereafter deliver individually designed participation programs using telehealth strategies. We will evaluate the effectiveness of the programs on reducing sedentary behaviours, increasing physical activity and increasing quality of life.
Detailed Description
This project will implement two intertwined strategies that will build the capacity of the carer, clinical and therapy communities to support physical activity in Rett syndrome. Individuals with Rett syndrome experience difficulties with movement and this can make it difficult to participate in regular physical activity. Individuals with Rett syndrome need support to participate in physical activities and it is important to work with primary caregivers when developing strategies to support physical activity. We will conduct a clinical trial that tests the effectiveness of working with primary caregivers to develop strategies suitable to their lives that aim to increase participation in physical activity in the individual with Rett syndrome whom they support. We will use a clinical trial design and work with primary caregivers using Telehealth. We will test whether this approach decreases sedentary time and increases physical activity. We will also test if there are changes in the sleep, behaviour and quality of life. We aim to recruit 60 families for this study, 26 of whom will live in Australia. Data from the three sites will be pooled for a stronger analysis. We acknowledge that physical activity can be associated with a fall and therefore our program will be developed with the primary caregiver to be suitable for their lives and capacity to provide support. However, by practicing more activity, the individuals with Rett syndrome could be stronger and risks of falling could be reduced. The risks for the individual with Rett syndrome are therefore low. To let the Rett syndrome community know our results, we will then develop an online resource documenting the physical activity program and the evidence available to support it, and this will be freely available to families, carers and therapists wherever they live in the world.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rett Syndrome
Keywords
Sedentary behaviour, Physical activity, Quality of life, Telehealth

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
We are using a waitlist controlled trial study design. Group membership will be determined using a concealed allocation randomisation after the baseline assessment. The 'immediate treatment' group will receive the 12-week intervention period following the assessment at baseline followed by a 12 week non-intervention period. The 'waitlist control' group receive no intervention in the first 12 week period and will then receive the intervention in the second 12 week period.
Masking
None (Open Label)
Masking Description
We note that our primary outcomes of sedentary behaviours and physical activity will be measured objectively by physical activity devices.
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Waitlist-Control Group
Arm Type
Experimental
Arm Description
The 'waitlist control' group will receive the 12-week non-intervention period first, followed by 12 week intervention period.
Arm Title
Immediate Treatment
Arm Type
Experimental
Arm Description
The 'immediate treatment' group will receive the 12-week intervention period first, followed by 12 week non-intervention period.
Intervention Type
Behavioral
Intervention Name(s)
Telehealth-delivered participation strategies to increase physical activity
Intervention Description
Therapists and primary caregivers will meet online on 6 occasions at fortnightly intervals over a 12 week period. Sessions will enable the development of strategies that will aim to increase the amount the participant stands and walks. Throughout, the therapists and primary caregivers will discuss physical activity needs, determine relevant activities, modify the program as necessary and plan additional goals.
Primary Outcome Measure Information:
Title
Average daily uptime (%)
Description
Percentage of time spent active (uptime) over total awake time, measured with an ActivPAL
Time Frame
Average over 4 days, data capture at baseline, after 12 weeks and after 24 weeks
Title
Average daily step count
Description
Number of daily steps measured by Stepwatch Activity Monitor
Time Frame
Average over 4 days, data capture at baseline, after 12 weeks and after 24 weeks
Secondary Outcome Measure Information:
Title
Sleep quality
Description
Sleep Disturbance Scale for Children.
Time Frame
Parent caregiver recall over previous month, data capture at baseline, after 12 weeks and after 24 weeks
Title
Behaviour
Description
Rett Syndrome Behaviour Scale
Time Frame
Parent caregiver recall over previous month, data capture at baseline, after 12 weeks and after 24 weeks
Title
Child Quality of Life
Description
Quality of Life Inventory-Disability (QI-Disability)
Time Frame
Parent caregiver recall over previous month, data capture at baseline, after 12 weeks and after 24 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Genetically confirmed Rett syndrome Able to stand (with or without assistance) Live in Australia, Denmark or Israel Exclusion Criteria: Individuals who have had spinal fusion over the previous 12 months Individuals who have had lower extremity orthopaedic surgery over the previous 6 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jenny Downs, PhD
Phone
+61 8 6319 1763
Email
Jenny.Downs@telethonkids.org.au
First Name & Middle Initial & Last Name or Official Title & Degree
Nicholas Buckley, BSc(Hons)
Phone
+61 8 6319 1771
Email
nicholas.buckley@telethonkids.org.au
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jenny Downs, PhD
Organizational Affiliation
Telethon Kids Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Rett Syndrom, Rigshospitalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michelle Stahlhut, PhD
Phone
+45 29 20 48 49
Email
michelle.stahlhut@regionh.dk
Facility Name
Ari'el University
City
Ari'el
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Meir Lotan, PhD
Email
ml_pt_rs@013net.net

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33376177
Citation
Downs J, Lotan M, Elefant C, Leonard H, Wong K, Buckley N, Stahlhut M. Implementing telehealth support to increase physical activity in girls and women with Rett syndrome-ActivRett: protocol for a waitlist randomised controlled trial. BMJ Open. 2020 Dec 29;10(12):e042446. doi: 10.1136/bmjopen-2020-042446.
Results Reference
derived

Learn more about this trial

Telehealth Support to Increase Physical Activity in Rett Syndrome

We'll reach out to this number within 24 hrs