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Mindfulness and wound healing.

Mindfulness and wound healing. - Mindfulness and wound healing

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON37957
Enrollment
66
Registered
2012-10-29
Start date
2012-11-07
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

n.v.t.: Onderzoek vindt plaats met gezonde mentaal capabele en wilsbekwame participanten. n.a.: Study will be carried out with healthy participants.

Interventions

Psychological intervention: The experimental group receives a standardized 8 week mindfulness intervention adopting the mindfulness based cognitive therapy (MBCT) protocol. The control group enters

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Age between 18 and 40 years old - Only participants who voluntarily signed up to follow a mindfulness training

Exclusion criteria

Exclusion criteria: - Self-reported health problems use that could influence cortisol levels, immune functioning and/or wound healing (e.g. auto-immune diseases, cancer, recent surgery, strokes, diabetes mellitus, peripheral vascular disease) -Self-reported medication use that could influence cortisol levels, immune functioning and/or wound healing (e.g. anti-diuretics, blood pressure regulators, psychotropic medication, anti-inflammatory drugs) - Other factors that may impact on cortisol levels, immune functioning and/or wound healing: self reported recreational drug use, heavy alcohol use (i.e. more than 10 alcoholic beverages per week for women and more than 20 for men), more than 10 units of caffeinated drinks per day - Psychopathological conditions / psychological treatment currently or over the past 6 months / previous psychiatric hospitalization (all self report) - Structural meditation practice (including yoga, tai chi, etc.) - Allergic responses to adhesives, bandages, or tapes, needle or blood phobias

Design outcomes

Primary

MeasureTime frame
Primary outcomes: Wound surface is determined by digital imaging of the wound 3 - 8 days post wound-induction; Reepithalisation is measured by comparing trans-epidermal water loss above the wound with taht above non damaged skin at 3-8 days .

Secondary

MeasureTime frame
Secondary outcomes/mediators: Cytokines IL-1a, IL-1β IL6, IL8, TNF-β) from wound exudate 3, 6, and 22 hours post wound-induction; Daily cortisol levels (AUC) and cortisol awakening response; Optimism and positive affect.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)