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An Approach to "Move a Little & Often" With Health Conditions

Primary Purpose

Depression, Multiple Chronic Conditions

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
A plan to Move a Little and Often
Sponsored by
University of Manchester
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Depression focused on measuring Sedentary Lifestyle

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • be aged ≥18 years,
  • self-report a clinical diagnosis of a long term physical health condition;
  • score 8 or more on the depression subscale of the Hospital hospital anxiety and depression scales (Zigmond & Snaith, 1983) suggesting the presence of depression;
  • speak English fluently;
  • live within Greater Manchester

Exclusion Criteria:

  • are not registered with a GP practice,
  • in receipt of palliative care,
  • report a diagnosis of severe mental health problems such as schizophrenia or bipolar disorder,
  • have had a recent bereavement

Sites / Locations

  • The University of Manchester
  • Salford Royal NHS Foundation Trust

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

A plan to Move a Little and Often

Arm Description

The intervention will consist of 3 components: a short video will raise awareness about the impact of sedentary behaviours, a booklet, and an online forum on Facebook to encourage participants to support each other. At the end of the baseline data collection, participants will be asked to watch the video. They will then be given the booklet and invited to join the Facebook group. A minimum of 5 participants must be recruited prior to running the Facebook group.

Outcomes

Primary Outcome Measures

The short form International Physical Activity Questionnaire (IPAQ ; Booth 2000).
The IPAQ will be used to measure frequency and duration of sedentariness, and any increase in physical activity. The IPAQ asks about walking, moderate intensity activities and vigorous-intensity activities. In order to compute the total score, it requires summation of the durations (minutes) and frequency (days) of walking, moderate-intensity and vigorous-intensity activities.

Secondary Outcome Measures

Full Information

First Posted
May 1, 2018
Last Updated
April 9, 2020
Sponsor
University of Manchester
Collaborators
NIHR CLAHRC
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1. Study Identification

Unique Protocol Identification Number
NCT03537053
Brief Title
An Approach to "Move a Little & Often" With Health Conditions
Official Title
Exploring the Acceptability of "Move a Little and Often"- a Behaviour Change Intervention to Reduce Sedentary Behaviours in People With Long Term Conditions and Symptoms of Depression.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
September 21, 2018 (Actual)
Primary Completion Date
July 20, 2019 (Actual)
Study Completion Date
July 20, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Manchester
Collaborators
NIHR CLAHRC

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
People with long term conditions such as diabetes and arthritis, and who also have depression spend a lot of time sedentary during the day. This is because they face many barriers to being active, such as pain and fatigue. Being sedentary is problematic because it is associated with poorer health in the long term. Common sedentary behaviours are watching television and using the computer; these behaviours are labelled as screen-based sedentary behaviours. An intervention to reduce these behaviours could improve mental and physical wellbeing. The aim of the study is to explore the acceptability of an intervention to "Move a Little and Often" in people with depression symptoms and long term conditions. The investigators will explore the intervention's acceptability using interviews and will examine if the intervention is associated with a reduction in time spent sedentary. Results will help refine the intervention further. The feasibility study is part of a PhD project funded by the National Institute of Health Research (NIHR) Collaborations for Leadership in Applied Health Research and Care (CLAHRC) Greater Manchester
Detailed Description
There is a growing focus in research on the need to reduce sedentary behaviours. Studies have shown that independently of moderate to vigorous physical activity, the amount of time spent sedentary predicts poorer health outcomes. This means that in addition to exercising, it is important to reduce prolonged periods of sedentary behaviours to improve health. For people with depression and long term conditions, milder forms of physical activity may be more appropriate due to higher levels of pain and fatigue resulting from exercise. Reducing sedentary behaviours by substituting them with mild physical activities such as walking is a potential avenue to improve health outcomes in this population group. To date, no intervention has been developed to reduce prolonged periods of sedentariness in people with depression and long term health conditions within the UK. This feasibility study aims to refine a behaviour change intervention to reduce sedentary time in this population group. The intervention has been developed through reviewing the literature on interventions to increase physical activity (a systematic review), an interview study to explore sedentary and physical activity behaviours within this population group, and through patient and public involvement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Multiple Chronic Conditions
Keywords
Sedentary Lifestyle

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
a single group feasibility study
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A plan to Move a Little and Often
Arm Type
Experimental
Arm Description
The intervention will consist of 3 components: a short video will raise awareness about the impact of sedentary behaviours, a booklet, and an online forum on Facebook to encourage participants to support each other. At the end of the baseline data collection, participants will be asked to watch the video. They will then be given the booklet and invited to join the Facebook group. A minimum of 5 participants must be recruited prior to running the Facebook group.
Intervention Type
Behavioral
Intervention Name(s)
A plan to Move a Little and Often
Intervention Description
The intervention content is reported using the behaviour change technique (BCT) Taxonomy v1 (Michie, et al. 2013). The video will contain the BCT: information about health consequences. The booklet will consist of BCTs: self-monitoring of behaviour, goal setting behaviour, action planning, commitment, social support (practical), self-talk, and mental rehearsal of successful performance. Lastly, usage of the Facebook group will include BCTs: commitment, and social support unspecified, practical and emotional. Mental rehearsal, goal setting behaviour and action planning will be delivered through mental simulation exercises (Taylor, et al. 1998). BCTs self-monitoring of behaviour, goal setting behaviour, and commitment will be delivered using implementation intentions (Gollwitzer 1993).
Primary Outcome Measure Information:
Title
The short form International Physical Activity Questionnaire (IPAQ ; Booth 2000).
Description
The IPAQ will be used to measure frequency and duration of sedentariness, and any increase in physical activity. The IPAQ asks about walking, moderate intensity activities and vigorous-intensity activities. In order to compute the total score, it requires summation of the durations (minutes) and frequency (days) of walking, moderate-intensity and vigorous-intensity activities.
Time Frame
1 month follow-up
Other Pre-specified Outcome Measures:
Title
Sedentary Behaviour Questionnaire (Gardiner, et al. 2011)
Description
The Sedentary Behaviour Questionnaire is a seven-item questionnaire that asks participants to report on activities they did during the last week while they were sitting or lying down, and to report the total time spent in each activity. The seven individual sedentary items are TV or video/DVD watching, computer use, reading, socializing with friends or family, time traveling in a motor vehicle or on public transport, doing hobbies, and any other activities they did while they were sitting or lying down. The measure has previously been used in a study of sedentariness in older adults (Gardiner, et al. 2011).
Time Frame
1 month follow-up
Title
The International Sedentary Assessment Tool (ISAT; Prince, et al. 2017)
Description
The ISAT contains 5 items relating to total time spent sedentary and time spent doing specific activities: television use, computer use, using transport, and reading. Participants will be asked how much time they spend on each activity over the course of a typical week. Psychometric properties have yet to be reported for this questionnaire measure.
Time Frame
1 month follow-up
Title
The Hospital Anxiety and Depression Scale (HADS; Zigmond and Snaith 1983)
Description
The HADS will measure depression and anxiety. The HADS is a 14-item self-report screening scale for anxiety and depression symptoms. It contains two 7 item scales: one for anxiety and one for depression; both of which have a score ranging from 0-21. The HADS is commonly used in research studies and has good validity (Bjelland et al. 2002, et al. 2005).
Time Frame
1 month follow-up
Title
The Numeric Rating Scale (NRS; Herr and Mobily 1993).
Description
Pain will be measured using the 0-10 Numeric Rating Scale (NRS) (Herr and Mobily 1993). Participants will be asked to rate their pain over the previous week. This questionnaire has been found to correlate significantly with other pain measures (Herr, et al. 2004). Scores can range from 0 to 10, with higher scores indicating more pain.
Time Frame
1 month follow-up
Title
The Pittsburgh Sleep Quality Index (Buysse, et al. 1989)
Description
Sleep quality and disturbances will be measured using the Pittsburgh Sleep Quality Index (Buysse, et al. 1989). The questionnaire can be used to generate seven component scores for subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleep medication, and daytime dysfunction. Each of the seven component scores is weighted equally on a scale of 0 (no difficulty) to 3 (severe difficulty). The seven component scores are then summed to yield a global PSQI score, ranging from 0 to 21, with a higher score indicating poorer sleep quality.
Time Frame
1 month follow-up
Title
The Measure of National Wellbeing (Carter 2017)
Description
Quality of life will be measured using items from the Measure of National Wellbeing used by the Office for National Statistics. Participants will be asked: overall, how satisfied they are with life nowadays; overall, to what extent they feel the things they do in life are worthwhile; overall, how happy they felt yesterday; overall, how anxious they felt yesterday?. Each question is answered on a scale of 0 to 10. People are asked to respond on a scale of 0 to 10, where 0 is "not at all" and 10 is "completely". Mean ratings for all 4 personal well-being questions will be calculated.
Time Frame
1 month follow-up
Title
Short Form Health Survey (SF-12; Ware, et al. 1996)
Description
The SF 12 is a 12 item measure with two scales: mental and physical functioning and overall health-related-quality of life. The SF-12 is weighted and summed to provide Physical and Mental Health Composite Scores (PCS & MCS). These two composite scores are computed using the scores of twelve questions and range from 0 to 100, where a zero score indicates the lowest level of health measured by the scales and 100 indicates the highest level of health. The questionnaire was adapted from the SF-36 Health Survey and its results can be compared with the SF36 (Jenkinson, et al. 1997)
Time Frame
1 month follow-up
Title
The ENRICHD Social Support Instrument (Mitchell, et al. 2003)
Description
Social support will be measured using the ENRICHD Social Support Instrument (Mitchell, et al. 2003). The ENRICHD Social Support Instrument (ESSI) is a brief seven-item measure of perceived social support. The scale contains six social support items that have been shown to be individually predictive of poor outcome in patients with cardiac disease, and one item that assesses partner status.
Time Frame
1 month follow-up
Title
The Self-Report Behavioural Automaticity Index SRBAI (Gardner, et al. 2012)
Description
The SRBAI will be used to measure habit strength for avoiding sedentariness. Participants will be asked to rate 4 items on a Likert scale of 0 (strongly disagree) to 5 (strongly agree). The 4 items are: avoiding being sedentary is something:- 1) I do automatically; 2) I do without having to consciously remember,3) I do without thinking, 4) I start doing before I realise I'm doing it.
Time Frame
1 month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: be aged ≥18 years, self-report a clinical diagnosis of a long term physical health condition; score 8 or more on the depression subscale of the Hospital hospital anxiety and depression scales (Zigmond & Snaith, 1983) suggesting the presence of depression; speak English fluently; live within Greater Manchester Exclusion Criteria: are not registered with a GP practice, in receipt of palliative care, report a diagnosis of severe mental health problems such as schizophrenia or bipolar disorder, have had a recent bereavement
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Isabel Adeyemi, MPhil
Organizational Affiliation
The University of Manchester
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Manchester
City
Manchester
ZIP/Postal Code
M13 9PL
Country
United Kingdom
Facility Name
Salford Royal NHS Foundation Trust
City
Manchester
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Anonymised data on demographics (age, gender) and standardised questionnaire measures will be shared.
IPD Sharing Time Frame
The data will become available upon publication of the study in an academic journal.

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An Approach to "Move a Little & Often" With Health Conditions

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