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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04351815
Other study ID # 2019_0011
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date December 20, 2019
Est. completion date March 11, 2022

Study information

Verified date August 2022
Source Hopital Foch
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aimed to evaluated the interest of a short-term (2 weeks) prehabilitation program compared to no prehabilitation before thoracic or urological surgery


Description:

Prehabilitation is a form of global strength training, aims to improve functional capacity before surgery.This preparation compensate for its decrease due to the intervention. This process includes physical training, nutritional and psychological care. Previous studies consider 4 weeks to be the ideal duration time for such program. However, extended program duration may reduce subject compliance and may not be possible for patient who can not or do not want to postponed their surgery.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date March 11, 2022
Est. primary completion date March 11, 2022
Accepts healthy volunteers No
Gender All
Age group 55 Years and older
Eligibility Inclusion Criteria: - Men or women aged 55 or over - Requiring major surgery (thoracic or urological surgery: kidney or bladder) within 15 days after the completion of the inclusion assessment - Having signed a consent form after a reflection period - Being affiliated to a Health Insurance plan. Exclusion Criteria: - Pregnant, parturient or lactating women - Persons deprived of their liberty: minors or adults subject to legal protection measures or out of state to express their consent - Patients (men or women) aged <55 years; - Inability to walk or initial physical assessment - Inability to complete questionnaires - Walk> 450 meters in the 6 minute test - Patients under guardianship or curators.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Short term prehabilitation (2 weeks)
Initial assessment visit with a dietitian, a psychologist, a physiotherapist, a doctor (physical medicine) and a geriatrician (for patients over 75 years old) Patient will be asked to follow a 2 weeks prehabilitation program 2 months post-surgery assessment visit with a dietitian, a psychologist, a physiotherapist, a doctor (physical medicine) 6 months post-surgery assessment visit with a dietitian, a psychologist, a physiotherapist, a doctor (physical medicine)
Other:
No specific intervention
Standard care: Initial assessment visit with a dietitian, a psychologist, a physiotherapist, a doctor (physical medicine) and a geriatrician (for patients over 75 years old) Patients will be asked to maintain regular physical activity without support 2 months post-surgery assessment visit with a dietitian, a psychologist, a physiotherapist, a doctor (physical medicine) 6 months post-surgery assessment visit with a dietitian, a psychologist, a physiotherapist, a doctor (physical medicine)

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Hopital Foch

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluated the change in physical condition of patient following a short prehabilitation compared to the initial assessment (6 minutes walk test) Change on the 6-minute walk test (distance covered over a time of 6 minutes in meters) 7 months
Primary Evaluated the change in physical condition of patient following a short prehabilitation compared to the initial assessment (Borg scale) Change in the Borg scale (exertion from 0 to 10: 0 meaning no exertion, 10 meaning maximal exertion) 7 months
Secondary Evaluated the change in cardio-respiratory capacity (VO2 max) of patient following a short prehabilitation at 15 days compared to the initial assessment VO2 Max Testing, measured in milliliters of oxygen used in one minute per kilogram of body weight (milliliter per kilogram per minute). 15 days
Secondary Evaluated the change in cardio-respiratory capacity (spirometry: maximal voluntary ventilation) of patient following a short prehabilitation at 15 days compared to the initial assessment Evolution of Maximal Voluntary Ventilation (MVV in liter per minute). 15 days
Secondary Evaluated the change in cardio-respiratory capacity (spirometry: vital capacity) of patient following a short prehabilitation at 15 days compared to the initial assessment Evolution of Vital Capacity (VC in liter) 15 days
Secondary Evaluated the change in cardio-respiratory capacity (spirometry: functional residual capacity) of patient following a short prehabilitation at 15 days compared to the initial assessment Evolution of Functional residual capacity (FRC in milliliter per kilogram). 15 days
Secondary Evaluated the change in cardio-respiratory capacity (heart rate) of patient following a short prehabilitation at 15 days compared to the initial assessment Heart rate at 40 watt during a cardiac stress test (beats per minute). 15 days
Secondary Evaluated the change in the muscular mass of patient following a short prehabilitation at 15 days compared to the initial assessment Quadriceps area in square centimeters. 15 days
Secondary Evaluated the change in the muscular strength of patient following a short prehabilitation at 15 days compared to the initial assessment Hand grip Test (measure in Newton). 15 days
Secondary Evaluated the change in the body mass (weight) of patient following a short prehabilitation at 15 days compared to the initial assessment Weight in kilogram. 15 days
Secondary Evaluated the change in the body mass (lean mass) of patient following a short prehabilitation at 15 days compared to the initial assessment Percentage of lean mass. 15 days
Secondary Evaluated the change on the psychological state (quality of life) of patient following a short prehabilitation at 15 days compared to the initial assessment SF-36 quality of life scale (eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. Each items are scored on a 0 to 100 range. A high score defines a more favorable health state). 15 days
Secondary Evaluated the change on the psychological state (anxiety and depression) of patient following a short prehabilitation at 15 days compared to the initial assessment Hospital Anxiety and Depression Scale (HADS)(a fourteen item scale that generates : Seven of the items relate to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 and 21 for either anxiety or depression). 15 days
Secondary Evaluated the change on the psychological state (fatigue) of patient following a short prehabilitation at 15 days compared to the initial assessment Patient-Reported Outcomes Measurement Information System (PROMIS) : PROMIS Fatigue-Short Form (seven items that measure both the experience of fatigue and the interference of fatigue on daily activities over the past week on a 5-point Likert scale, ranging from 1 = never to 5 = always). 15 days
Secondary Evaluated the change on the psychological state (sleep) of patient following a short prehabilitation at 15 days compared to the initial assessment Patient-Reported Outcomes Measurement Information System (PROMIS): PROMIS-Sleep Disturbance-Short Form (eight items that measure both the experience problems with sleep and the interference of problems with sleep on daily activities over the past week, ranging from 1 = not at all to 5 = very much). 15 days
Secondary Evaluated the change on the psychological state (pain) of patient following a short prehabilitation at 15 days compared to the initial assessment Patient-Reported Outcomes Measurement Information System (PROMIS): PROMIS Pain Interference - Short Form (six items that measure both the experience of pain and the interference of pain on daily activities over the past week, ranging from 1 = not at all to 5 = very much). 15 days
Secondary Evaluated the change on the psychological state (geriatric health) of patient following a short prehabilitation at 15 days compared to the initial assessment Geriatric health status screening tool (G8 score) (8 questions score between 0 and 17, a higher score indicates a better health status). For geriatric patient only. 15 days
Secondary Evaluated the change on the psychological state (daily living) of patient following a short prehabilitation at 15 days compared to the initial assessment Instrumental activities of daily living scale (8 domains of function ranges from 0 (low function, dependent) to 8 (high function, independent)) 15 days
Secondary Evaluate compliance to the prehabilitation program Overall compliance score regarding physical training, proteins intake, well-being and fatigue (complete, partial or non compliance). 15 days
Secondary Evaluate post-surgery complications (classification) Classification of complications according to Dindo and Clavien (grades I, II, IIIa, IIIb, IVa, IVb or V). 2 months and 6 months
Secondary Evaluate post-surgery complications (length of stay) Length of stay in hospital, in intensive care unit or continuous monitoring unit (number of days). 2 months and 6 months
Secondary Evaluate post-surgery complications (mortality) Hospital and 30-day mortality (patient status). 2 months and 6 months
Secondary Evaluate post-surgery complications (re-hospitalization) Re-hospitalization in the same hospital within 30 days of discharge from the initial hospitalization (yes/no). 2 months and 6 months
Secondary Evaluate post-surgery complications : comparison between predicted complications and actual complications (ARISCAT) ARISCAT score (risk of postoperative respiratory complication considered to be low for a score less than 26, moderate for a score of 26 to 44, and high for a score of 45 or more). 2 months and 6 months
Secondary Evaluate post-surgery complications : comparison between predicted complications and actual complications (LEE) LEE score (postoperative cardiac risk (infarction, heart failure, death): 0-1 low risk, 2 significant risk, more than 3 major risk). 2 months and 6 months
Secondary Evaluate post-surgery complications : comparison between predicted complications and actual complications (POSPOM) Preoperative Score To Predict Postoperative Mortality (POSPOM) system (scale of 0 to 50 points, with 0 given to patients with the lowest risk). 2 months and 6 months
Secondary Evaluate post-surgery complications : comparison between predicted complications and actual complications (Charlson index) Charlson index (22 conditions are assigned a score of 1, 2, 3, or 6, depending on the risk of dying associated with each one. Scores are summed to provide a total score to predict mortality. A higher score indicates a higher risk of mortality.) 2 months and 6 months
Secondary Evaluate post-surgery complications : comparison between predicted complications and actual complications (POSSUM score) Physiologic and Operative Severity Score for the enUmeration of Mortality and Morbidity score (POSSUM score) (18 factors scored exponentially increasing from 1 to 8. A higher score indicates a higher risk of mortality). 2 months and 6 months
Secondary Evaluated the change in cardio-respiratory capacity (6 minutes walk test) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Change on the 6-minute walk test (distance covered over a time of 6 minutes in meters). 2 months and 6 months
Secondary Evaluated the change in cardio-respiratory capacity (VO2 max) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment VO2 Max Testing, measured in milliliters of oxygen used in one minute per kilogram of body weight (milliliter per kilogram per minute). 2 months and 6 months
Secondary Evaluated the change in cardio-respiratory capacity (spirometry: maximal voluntary ventilation) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Evolution of Maximal Voluntary Ventilation (MVV in liter per minute). 2 months and 6 months
Secondary Evaluated the change in cardio-respiratory capacity (spirometry: vital capacity) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Evolution of Vital Capacity (VC in liter). 2 months and 6 months
Secondary Evaluated the change in cardio-respiratory capacity (spirometry: functional residual capacity) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Evolution of Functional residual capacity (FRC in milliliter per kilogram). 2 months and 6 months
Secondary Evaluated the change in cardio-respiratory capacity (heart rate) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Heart rate at 40 watt during a cardiac stress test (beats per minute). 2 months and 6 months
Secondary Evaluated the change in the muscular mass of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Quadriceps area in square centimeters. 2 months and 6 months
Secondary Evaluated the change in the muscular strength of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Hand grip Test (measure in Newton). 2 months and 6 months
Secondary Evaluated the change in the body mass (weight) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Weight in kilogram. 2 months and 6 months
Secondary Evaluated the change in the body mass (lean mass) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Percentage of lean mass. 2 months and 6 months
Secondary Evaluated the change on the psychological state (quality of life) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment SF-36 quality of life scale (eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. Each items are scored on a 0 to 100 range. A high score defines a more favorable health state). 2 months and 6 months
Secondary Evaluated the change on the psychological state (anxiety and depression) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Hospital Anxiety and Depression Scale (HADS) (a fourteen item scale that generates : Seven of the items relate to anxiety and seven relate to depression. Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 and 21 for either anxiety or depression). 2 months and 6 months
Secondary Evaluated the change on the psychological state (fatigue) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Patient-Reported Outcomes Measurement Information System (PROMIS) : PROMIS Fatigue-Short Form (seven items that measure both the experience of fatigue and the interference of fatigue on daily activities over the past week on a 5-point Likert scale, ranging from 1 = never to 5 = always). 2 months and 6 months
Secondary Evaluated the change on the psychological state (sleep) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Patient-Reported Outcomes Measurement Information System (PROMIS): PROMIS-Sleep Disturbance-Short Form (eight items that measure both the experience problems with sleep and the interference of problems with sleep on daily activities over the past week, ranging from 1 = not at all to 5 = very much) 2 months and 6 months
Secondary Evaluated the change on the psychological state (pain) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Patient-Reported Outcomes Measurement Information System (PROMIS): PROMIS Pain Interference - Short Form (six items that measure both the experience of pain and the interference of pain on daily activities over the past week, ranging from 1 = not at all to 5 = very much). 2 months and 6 months
Secondary Evaluated the change on the psychological state (geriatric health) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Geriatric health status screening tool (G8 score) (8 questions score between 0 and 17, a higher score indicates a better health status). For geriatric patient only. 2 months and 6 months
Secondary Evaluated the change on the psychological state (daily living) of patient following a short prehabilitation at 2 and 6 months compared to the initial assessment Instrumental activities of daily living scale (8 domains of function ranges from 0 (low function, dependent) to 8 (high function, independent)). 2 months and 6 months
Secondary Evaluated the compliance to the prehabilitation program Overall compliance score regarding physical training, proteins intake, well-being and fatigue (complete, partial or non compliance) 2 months and 6 months
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