- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT02869854
Increased Physical Activity Through Mindfulness (FAR-MIND)
Increased Adherence to Physical Activity on Prescription (PAP) Through Mindfulness- A Pilot Study.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
All patients between 40 and 65 years of age who fulfills the inclusion criteria will be asked to participate in the study. Posters with information about the study will be put in the waiting room and on other strategic places. Patients who accept to participate will get both written and orally information, after the information they will sign a informed consent. The patients will estimate their level of physical activity in minutes per week to control inclusion criteria. The patients will return a morning for fasting blood samples and get an accelerometer attached to them to wear during 7 days. During this time randomization will be preformed. They will also get to answer a couple of different surveys. The results from the surveys and blood samples will be the study baseline.
All patients with abnormal test results will follow specific flow diagram for the usual care.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Skane
-
Malmö, Skane, Schweden, 205 02
- Lunds Unniversitet
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Individuals between 40-65 years of age, with insufficient physical activity ( <150 minutes of moderate-intensity physical activity throughout the week, or < 75 minutes of vigorous-intensity physical activity throughout the week, or an equivalent combination of moderate- and vigorous-intensity activity.)
Exclusion Criteria:
- Dementia, severe mental disorder,newly diagnosed untreated unstable angina pectoris,myocardial infarction within 6 weeks prior to study entry. Individuals who do not master the Swedish language in speech and writing will be excluded.The patients who have abnormal values according to guidelines that require contact with a physician on the same day or week will also be excluded
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
---|---|
Aktiver Komparator: PAP only
This group will follow the referral scheme for three months, and after this period they will leave new blood samples and answer surveys.
They will get a new PAP with follow up after another 3 months.
|
Physical Activity on Prescription, after 3 months a new prescription
|
Aktiver Komparator: Mindfulness only
Mindfulness.
This group will receive a group course in mindfulness during 8 weeks once a week, and with 20 minutes of daily personal training.
Three and six months after inclusion they will answer a new set of surveys and fasting blood samples.
|
Mindfulness course during 8 weeks with 20 minutes mindfulness exercise each day
|
Experimental: Combination of the two groups
Mindfulness and physical activity prescription.
This group will get a combination of the two other groups.
PAP will be prescribed during the first meeting and another one after 3 months.
During the first 8 weeks once a week they will participate in a mindfulness training group and also preform 20 minutes of daily training.
The same surveys as the other groups and fasting blood samples
|
Physical Activity on Prescription, after 3 months a new prescription
Mindfulness course during 8 weeks with 20 minutes mindfulness exercise each day
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Difference of time, measured in minutes of activity during a week, between the three different groups measured by activity monitor Actigraph (GT3X)
Zeitfenster: 6 months
|
Each individual will wear an activity monitor during 7 days.
This will be done at baseline after 3 months and after 6 months
|
6 months
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Difference between the three groups in revised assessment of their self-rated health and
Zeitfenster: 6 months
|
assessment based on terms of perceived health with five alternative answers very poor, poor, fair, good and very good
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6 months
|
Difference between groups in the amount of self-perceived sleep problems
Zeitfenster: 6 months
|
Insomnia Severity Index(ISI); is a self-report questionnaire measuring insomnia symptoms to evaluate the degree of insomnia.
The scale consists of seven questions that evaluate Sleep mode , sleep during the night , waking up early , feeling of being rested, how sleeping problems affecting daily life , and how sleep patterns concern the individual
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6 months
|
Differences between the three intervention groups regarding change in biomarkers such as proteins , micro - RNA , cytokines, mitochondrial DNA and telomeres
Zeitfenster: 6 months
|
blood samples
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6 months
|
Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Ermittler
- Hauptermittler: Bengt Zöller, Docent, Lunds University
Publikationen und hilfreiche Links
Allgemeine Veröffentlichungen
- Nymberg P, Ekvall Hansson E, Stenman E, Calling S, Sundquist K, Sundquist J, Zoller B. Pilot study on increased adherence to physical activity on prescription (PAP) through mindfulness: study protocol. Trials. 2018 Oct 17;19(1):563. doi: 10.1186/s13063-018-2932-9.
- Nymberg P, Calling S, Stenman E, Palmer K, Hansson EE, Sundquist K, Sundquist J, Zoller B. Effect of mindfulness on physical activity in primary healthcare patients: a randomised controlled trial pilot study. Pilot Feasibility Stud. 2021 Mar 17;7(1):70. doi: 10.1186/s40814-021-00810-6.
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
- Pny1
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
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