PAPRIKA - Patients Empowerment for Major Surgery Preparation @Home

Sponsor
Hospital Clinic of Barcelona (Other)
Overall Status
Unknown status
CT.gov ID
NCT04295668
Collaborator
(none)
300
1
6.9
43.3

Study Details

Study Description

Brief Summary

PAPRIKA establishes a technologically enabled and personalized prehabilitation and follow-up after surgical intervention program for patients undergoing elective major surgery Program creates close collaboration between the medical environment and the patients empowering them to co-create their own care.

It is at the first stage aimed to high-risk patients undergoing major surgery. Better condition before the surgery is proved to reduce the perioperative complications and to improve patients' health-related quality of life while cutting the associated costs. The concept integrates short-term (average 4 weeks) preoperative interventions including endurance training, promotion of physical activity and nutritional and psychological support. Interventions are planned both at community and at hospital reducing unnecessary interactions between patients and tertiary care.

PAPRIKA tackles three major drivers: i) human perspective ii) organizational challenges and

  1. technical aspects. The project is based on previous experience on prehabilitation and the already refined service using design thinking methodologies. It will be also based on the proven reduction of associated costs for the healthcare system.
Condition or Disease Intervention/Treatment Phase
  • Behavioral: Usual care
  • Behavioral: Prehabilitation

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
300 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
PAPRIKA - Patients Empowerment for Major Surgery Preparation @Home
Actual Study Start Date :
Jan 1, 2020
Anticipated Primary Completion Date :
Jun 30, 2020
Anticipated Study Completion Date :
Jul 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Usual care

A contemporaneous control group of patients was build using propensity score matching (PSM) methodologies taking into account the following matching variables: type of surgery, age, sex, American Society of Anesthesiologists Index (ASA) and adjusted morbidity groups (GMA) grading.

Behavioral: Usual care
The preoperative standard measures consist of physical activity recommendation and advice on both smoking cessation and alcohol intake reduction. Moreover, in patients presenting with anemia, the anesthesiologists will assess its etiology and treat it accordingly, and nutritional intervention will be performed by a registered dietitian in to those patients at risk of malnutrition (Malnutrition Universal Screening Tool ≥2).

Prehabilitation

Prospective sample of risk patients who are candidates for major surgery attended in the outpatient offices of the Hospital Clínic de Barcelona. Inclusion criteria: i) American Society of Anesthesiologists Index (ASA) 3-4; and / or, ii) age ≥ 75 years; and / or iii) major aggressive surgery; and, iv) solid organ transplant candidate. Exclusion criteria: i) Non-elective surgery; ii) Known metastatic disease before surgery; iii) Unstable respiratory or heart disease; or, iv) Locomotive or cognitive limitations that prevent adherence to the program.

Behavioral: Prehabilitation
i) Exercise training: Ambulatory exercise training sessions with two main components, namely: high-intensity endurance exercise training and strength muscular training. ii) Promotion of physical activity: Pedometer-based program using a physical activity tracker linked to a mobile app. iv) Nutritional optimization: Recommendations of a healthy balanced diet or adapted to their digestive symptoms. Daily amount of protein intake will be close to 2 g•Kg-1•day-1. iv) Smoking cessation: Use of both cognitive behavioral intervention and pharmacological therapy by varenicline or nicotine replacement therapies. v) Cognitive behavioral therapy: Weekly group sessions conducted by a clinical health psychologist, including psychoeducation, motivational and behavioral change, self-efficacy and adherence enhancement, coping strategies acquisition and patient empowerment.

Outcome Measures

Primary Outcome Measures

  1. Postoperative complications [Duration of the initial hospitalization for surgery]

    Number of postoperative complications during the initial hospitalization for surgery

  2. Hospital length of stay [Duration of the initial hospitalization for surgery]

    Number of days of hospital length of stay during the initial hospitalization for surgery

  3. Severity of postoperative complications [Duration of the initial hospitalization for surgery]

    Severity of postoperative complications during the initial hospitalization for surgery using the Clavien-Dindo classification

Secondary Outcome Measures

  1. Hospital readmissions at 30 days [From initial hospital discharge to 30 days follow-up]

    Number of postoperative complications during a 30-day period after surgery

  2. Emergency room visits at 30 days [From initial hospital discharge to 30 days follow-up]

    Number of emergency room visits during a 30-day period after surgery

  3. Surgical reinterventions at 30 days [From initial hospital discharge to 30 days follow-up]

    Number of surgical reinterventions during a 30-day period after surgery

  4. Mortality at 30 days [From initial hospital discharge to 30 days follow-up]

    Number of exitus during a 30-day period after surgery

Other Outcome Measures

  1. Six-minute walk test [At program inclusion and at program discharge (on average at 6 weeks)]

    Distance covered during the six-minute walk test

  2. Physical activity [At program inclusion and at program discharge (on average at 6 weeks)]

    Physical activity measured by the Yale Physical Activity Survey (YPAS) (range 0 to 142; the lowest the worst)

  3. Psycho-emotional status [At program inclusion and at program discharge (on average at 6 weeks)]

    Psycho-emotional status measured by the Hospital Anxiety and Depression (HAD) scale (range 0-21; the highest the worst)

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age > 70 years old and/or American Society of Anesthesiologist (ASA) index 3-4 and/or highly aggressive surgery or solid organ transplantation.
Exclusion Criteria:
  • Non-elective surgery; metastatic disease.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital Clínic de Barcelona Barcelona Catalonia Spain 08036

Sponsors and Collaborators

  • Hospital Clinic of Barcelona

Investigators

  • Study Director: Josep Roca, Prof, Hospital Clinic of Barcelona

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Anael Barberan-Garcia, Principal investigator, Hospital Clinic of Barcelona
ClinicalTrials.gov Identifier:
NCT04295668
Other Study ID Numbers:
  • HCB/2019/1030
First Posted:
Mar 4, 2020
Last Update Posted:
Mar 4, 2020
Last Verified:
Mar 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Anael Barberan-Garcia, Principal investigator, Hospital Clinic of Barcelona

Study Results

No Results Posted as of Mar 4, 2020