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Randomized controlled, three-arm parallel group, clinical trial on efficacy and safety of rhythmic embrocations on post-surgical stress in colorectal cancer patients


ABSTRACT: Interventions: Group 1: Rhythmical Embrocations (RE) performed by experts: Every RE will be performed using pure almond oil (approx. 2 mL per treatment) in the morning (between 8 and 10 pm) and the evening (between 6 and 10pm) for approx. 10 minutes. Regarding intensity of the massage the treatment of the back will use intensities between 1-3 and the treatment of the back will use intensities between 1-5 (on a scale of 1=softest massage possible” and 10=very intense massage”). The patients are asked to rest for 20 minutes after the embrocation. Staff and patients in the same room will be informed about the intervention and resting time orally and by a sign at the patient’s door signaling ‘study intervention, please do not disturb until x:xx’ and will be asked not to interrupt during these periods. 1. RE of the back in the morning: The patient is sitting at the bedside and leaning with his arms on a nightstand or over a pillow; safe sitting has to be achieved in this position as an obligatory prerequisite for this treatment. During this treatment, only one hand is touching the patient at one time. The treatment can be described as two different movements: in the first movement the hand is moved in circles over one side of the back with the circles going down; the circles are clockwise at the left side of the back and anti-clockwise at the right side of the back; there is a slightly stronger touch when going down above the M. erector spinae to the middle of back (the spine is not touched within these movements); the second movement is a line on one side of the back and then the other going down. Every movement is repeated about 3 times on every side of the back. 2. RE of the feet in the evening: The patient is lying in his bed with a knee roll under his knees (or something simi Primary outcome(s): Stress as measured with heart rate variability (SDNN) on day 6 (after last treatment) Study Design: Allocation: Randomized controlled study; Masking: Open (masking not used); Control: active; Assignment: parallel; Study design purpose: supportive care

DISEASE(S): Malignant Neoplasm Of Rectum,Malignant Neoplasm Of Rectosigmoid Junction,Malignant Neoplasm Of Colon

PROVIDER: 2438044 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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