Strategies Empowering Activities in Everyday Life (SEE 1.0) a Web-based Occupational Therapy Intervention

August 29, 2024 updated by: Maria Larsson Lund, Luleå Tekniska Universitet

Strategies Empowering Activities in Everyday Life (SEE 1.0): a Study Protocol for a Feasibility Trial of a Web-based Occupational Therapy Intervention for People with Stroke

The purpose of the study is to evaluate the feasibility and potential outcomes of a first version of a web-based intervention in occupational therapy focusing on empowering an active everyday life for people with stroke.

Study Overview

Status

Completed

Conditions

Detailed Description

A large amount of people with stroke face extensive changes to live an active life and restrictions in engaging in various activities are common. However, the rehabilitation seldom focusses on the process of change people with stroke need to go through to adapt to their changed capacity and reach an active life on new terms. This implies that rehabilitation needs to be developed to provide activity-based self-management strategies that can facilitate an active life. Also, there is a need to improve the access to rehabilitation by making use of digital e- health solutions. Based on these needs, the web-based occupational therapy intervention "Strategies Empowering activities in Everyday life" (SEE 1.0) has been developed.

This feasibility trial has a pre-test post-test design without a control group. The trial is embedded in a mix- method approach combining assessment tools, feasibility registration forms, intervention logbooks, qualitative interviews and focus groups. The feasibility of the web-based intervention SEE as well as of the study design, will be evaluated in terms of acceptability, adherence, values and appropriateness from the perspectives of patients with stroke and the staff. Also, the potential outcome of SEE will be evaluated quantitatively and qualitatively.

The results will support the continued development of SEE and provide for larger-scale research studies. The intervention, that combines a focus on empowering an active everyday life with a web-based format including online meetings, is innovative and is not part of clinical practice today. Thereby, the results can be valuable for future research and clinical practice in general. The study protocol and the results will be published in peer-reviewed scientific journals and presented at conferences.

Study Type

Interventional

Enrollment (Actual)

15

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Luleå, Sweden, 97187
        • Department of Health Science, LTU

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Stroke
  • Age: 18-75 years
  • three to thirty six months after the onset of the stroke
  • have moderate disability or good recovery after the stroke
  • have access to a screen/computer, internet and e-ID as well as being able to use them
  • experience limitations in activities in everyday life
  • be motivated to participate in the program, including be ready for a process of change
  • be discharged from rehabilitation at hospital or day care.

Exclusion Criteria:

  • depression
  • other conditions or diseases that impact on activities in everyday life
  • have impairments or other diagnoses to such an extent that may have an impact on the ability to consent participation as well as participate in the data collection and intervention.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: The web- based occupational therapy intervention SEE
The web-based intervention starts with eight educational modules focusing on engagement in activities and strategies to support an active life. The modules, that is delivered on a secure national health platform, include short education videos followed by self-reflections and digital assignments supporting the change process. The occupational therapist provides feedback after each assignment and, also, meet the patients for face- to- face online guiding sessions at three times during these first two- three weeks of the intervention. Thereafter, an individually tailored activity plan with goals and activity-based strategies are established. During the change process, the patients receive continued support from the occupational therapist until the goals are achieved.

The patients are provided a person-centered activity-based intervention on the web aiming at facilitating the level of engagement in a variety of activities, at different places in society, together with other people to support an active life. In the long-term, the change to an active life will be reflected in a healthy and balanced pattern of activities.

The program provide the patients with tools to "see" their activities in everyday life in a new light and, also, tools to identify activity-based strategies that can empower them to take an active role to prevent and overcome challenging situations in everyday life.

Other Names:
  • Strategies Empowering activities in Everyday life (SEE 1.0) A web-based occupational therapy intervention for people with stroke

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The profiles of occupational engagement (POES)
Time Frame: Change from baseline to four- and twelve-months post-base line.
Change in activity pattern/profile.The POES is based on an interview of an 24 h completed diary of time use. The nine items are scored on an ordinal scale ranging from 1 to 4. A higher score indicates a higher level of engagement in activities.
Change from baseline to four- and twelve-months post-base line.
Occupational Balance Questionnaire (OBQ)
Time Frame: Change from baseline to four- and twelve-months post-base line
Change in occupational balance, reflecting a person's subjective perception of having the right amount of activities and the right variation between activities. The OBQ consist of 11 items that are rated on a four-point ordinal scale, scored 0 to 3. The ratings of the OBQ are summed to a total score, ranging between 0 and 33. A higher score implies more satisfaction with the amount and variation of occupations, i.e., a higher level of occupational balance.
Change from baseline to four- and twelve-months post-base line
Occupational values with pre-defined items (Oval-pd).
Time Frame: Change from baseline to four- and twelve-months post-base line
Change in occupational values, reflecting a person's subjective perception of concrete, symbolic or self-rewarding values in activities. The OVal-pd consists of 18 items rated on a four-point ordinal scale with response options scored 1 to 4. The rating of the OVal-pd can be summed into a general occupational value, ranging between 18-72. .A higher score indicates that the respondent is frequently engaged in valued occupation.
Change from baseline to four- and twelve-months post-base line

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Life satisfaction questionnaire (Lisat-11)
Time Frame: Change from baseline to four- and twelve-months post-base line
Change in life satisfaction. The Life satisfaction questionnaire consist of 11 items rated on a six-point ordinal scale ranging from 1 to 6. A higher score reflects a higher level of satisfaction.
Change from baseline to four- and twelve-months post-base line
The general self- efficacy scale (S-GSE)
Time Frame: Change from baseline to four- and twelve-months post-base line
Change in general self- efficacy. The S-GSE consist of 10 items that are rated on a four-point ordinal scale, ranging from 1 to 4. The summarized score range between 10-40. A higher score reflects greater sense of general self-efficacy.
Change from baseline to four- and twelve-months post-base line
Work ability index (WAI)
Time Frame: Change from baseline to four- and twelve-months post-base line
Change in self-perceived work ability. In the WAI, self-perceived work ability is rated on a ten -point ordinal scale. A higher score reflects a higher level of perceived work ability.
Change from baseline to four- and twelve-months post-base line
Stroke Impact Scale, participation (SIS)
Time Frame: Change from baseline to four- and twelve-months post-base line
Change in impact of stroke on participation is rated on a five-point ordinal scale. A higher score reflects a higher level of participation
Change from baseline to four- and twelve-months post-base line

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
The clients' (own) experiences of adopting activity-based strategies during the intervention process of SEE and the influence of these for an active life
Time Frame: Repeatedly interviews during the intervention process, one- and fourth months post- baseline
Experiences of adopting activity-based strategies during the intervention process of the SEE and the influence of these for an active life will be explored by qualitative interviews
Repeatedly interviews during the intervention process, one- and fourth months post- baseline
The acceptability and value of the the SEE from the perspective of the receivers
Time Frame: Four- and twelve months post- baseline
The acceptability and value of the SEE from the perspective of the receivers will be studied with a study specific questionnaire. The items are rated on four-graded ordinal scale, ranging from 1 to 4. Higher scores reflect higher levels of acceptability and values of the SEE.
Four- and twelve months post- baseline
The adherence of the SEE
Time Frame: During each patient's intervention process, every planned intervention occasion (according to the intervention guide), up to twelve months post-base line.
The adherence of the SEE will be studied with a study specific feasibility registration form assessing whether the intervention is delivered and taken as intended.
During each patient's intervention process, every planned intervention occasion (according to the intervention guide), up to twelve months post-base line.
The acceptability and value of the SEE from the perspective of the delivers
Time Frame: Every fourth month during the study period of two years.
Experiences of the SEE from the perspectives of the delivers, i.e., the occupational therapists, their managers and other stakeholders/key persons will be explored qualitatively in focus groups.
Every fourth month during the study period of two years.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Maria A Larsson-Lund, Prof, Luleå University of Technology

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2020

Primary Completion (Actual)

June 30, 2023

Study Completion (Actual)

June 30, 2023

Study Registration Dates

First Submitted

October 2, 2020

First Submitted That Met QC Criteria

October 8, 2020

First Posted (Actual)

October 19, 2020

Study Record Updates

Last Update Posted (Actual)

September 3, 2024

Last Update Submitted That Met QC Criteria

August 29, 2024

Last Verified

August 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Due to Swedish law, acts and regulations it is not possible to share data open. Data are archived at Luleå university of technology. Request for access the data can be sent to registrator@ltu.se

IPD Sharing Time Frame

Then the project is finished and results are published in international journals, anticipated 2024

IPD Sharing Access Criteria

The datasets will be stored anonymous and access will be possible on reasonable request after the project is finished.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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