REcovery After Cancer Application
NCT07642492 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 250
Last updated 2026-08-05
Summary
The RECapp study is a clinical trial evaluating a digital tool designed to support patients recovering from surgery for oesophageal or stomach cancer. The goal is to reduce symptoms and improve quality of life during recovery.
Each year in Sweden, around 1,400 people are diagnosed with these cancers. Although more people are surviving thanks to better treatments, recovery after surgery is often long and challenging, with lasting physical and emotional effects. At the same time, healthcare systems are under pressure to provide long-term support.
RECapp is a digital platform developed together with patients and healthcare professionals. It includes a mobile app for patients and a web portal for healthcare staff. Patients can track their symptoms, receive personalised self-care advice, and get guidance on when to contact healthcare. Healthcare providers can follow patients' progress remotely.
In this study, 250 patients from across Sweden will take part. They will be randomly assigned to either standard care or standard care plus RECapp. Participants will be followed for six months after surgery, and their symptoms and quality of life will be regularly assessed through questionnaires.
If RECapp proves effective, it could become part of future cancer care in Sweden-helping patients feel better supported while also making care more efficient.
Conditions
- Oesophageal Cancer
- Gastric Cancer (Diagnosis)
Interventions
- DEVICE
-
The RECapp platform
The RECapp platform is a device for oesophageal and gastric cancer patients having undergone invasive surgery as part of the curatively intended treatment regime. It is designed to improve recovery and mitigate symptom burden. The RECapp platform includes a mobile application to be used by patients, the RECapp app, and a web application system to be used by healthcare providers, the RECapp care portal. The RECapp app tracks symptom burden through questionnaires, provides feedback on individual status, and provides self-care advice or alerts patients to contact healthcare based on self-reported symptom burden. The RECapp care portal provides healthcare providers with access to the patients' reported history. The RECapp app is to be used by the patient at home, and the RECapp care portal is to be used by healthcare providers in a healthcare setting.
Sponsors & Collaborators
-
Karolinska Trial Alliance
collaborator INDUSTRY - lead OTHER
Principal Investigators
-
Pernilla Lagergren, Professor · Surgical care science, Molecular Medicine and Surgery, Karolinska Institute
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-09-15
- Primary Completion
- 2029-12-15
- Completion
- 2029-12-15
Countries
- Sweden
Study Locations
More Related Trials
-
Dissemination and Implementation of DIGEST™ as an Evidence-based Measurement Tool for Dysphagia: A Randomized Implementation Trial
NCT07283653 ·Status: RECRUITING ·Phase: NA
-
Esophageal Stump Washout
NCT01980394 ·Status: COMPLETED ·Phase: NA
-
Partial Versus Total Fundoplication in the Surgical Repair of Para-esophageal Hernia.
NCT04436159 ·Status: COMPLETED ·Phase: NA
-
Paracetamol Absorption Technique as a Method for Measuring Gastric Tube Outlet
NCT02158286 ·Status: COMPLETED
-
Surveillance and Image-Guided Biopsy of the Esophagus Using an OFDI Capsule
NCT02422433 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Comparison of Captivator Tissue Cassettes vs. no Cassettes for Endoscopic Mucosal Resection in Esophageal Carcinoma
NCT02911363 ·Status: COMPLETED ·Phase: NA
-
Local Metabolism of the Gastric Tube Reconstruction After Esophagectomy
NCT04319835 ·Status: COMPLETED ·Phase: NA
-
Stretta Treatment in GERD After SG
NCT05094895 ·Status: UNKNOWN ·Phase: NA
-
Comparison of Total and Partial Fundoplication During Surgery of Patients With Gastroesophageal Reflux Disease
NCT03659487 ·Status: COMPLETED ·Phase: NA
-
EndoVE endosCopic Treatment for Oesophageal and Gastric canceR
NCT04649372 ·Status: COMPLETED ·Phase: NA
-
Capsule Endoscopy for Post-Ablation Esophageal Lesion Assessment
NCT00990782 ·Status: COMPLETED ·Phase: NA
-
Botulinum Toxin Type A in Preventing Complications After Surgery in Patients With Esophageal Cancer
NCT02965976 ·Status: COMPLETED ·Phase: PHASE2
-
Effect of Feeding Jejunostomy on Sarcopenia in Patients With Esophageal Cancer
NCT06712706 ·Status: ACTIVE_NOT_RECRUITING
-
Assessment of Graft Perfusion and Oxygenation for Improved Outcome in Esophageal Cancer Surgery
NCT03587532 ·Status: RECRUITING ·Phase: NA
-
Minimally Invasive Molecular Approaches for the Diagnosis of Barrett's Esophagus and Esophageal Adenocarcinoma
NCT03961945 ·Status: RECRUITING ·Phase: NA
-
Focal Cryoballoon Ablation for Malignant Dysphagia
NCT06618742 ·Status: RECRUITING ·Phase: NA
-
Plastic Stents Compared With Metal Stents in Treating Patients With Malignant Dysphagia Caused by Esophageal Cancer or Gastroesophageal Junction Cancer
NCT00372450 ·Status: WITHDRAWN ·Phase: NA
-
Bougiecap for Treatment of Benign Stenosis in GI Tract
NCT03349021 ·Status: COMPLETED ·Phase: NA
-
Swedish Oesophago-Gastric Study
NCT05540119 ·Status: UNKNOWN
-
Pharyngeal Electrical Stimulation for the Treatment of Post-extubation Dysphagia in Acute Stroke
NCT02470078 ·Status: COMPLETED ·Phase: NA
-
Comparative Study Between (FC-SEMS) and (PC-SEMS) in the Palliation of Dysphagia Due to Malignant Neoplasm of Esophagus.
NCT06070376 ·Status: RECRUITING ·Phase: NA
-
The Application of Symptoms Management Program Based on the Patient Reported Outcome After Esophagectomy
NCT07187154 ·Status: RECRUITING ·Phase: NA
-
WavSTAT® Optical Biopsy System to Target Esophageal Biopsies
NCT00747136 ·Status: TERMINATED
-
Perioperative Perfusion Measurement - a Feasibility and Usability Study
NCT03671642 ·Status: COMPLETED ·Phase: NA
-
Register Study: Implementation of Pharyngeal Electrostimulation Therapy for the Treatment of Acute Neurogenic Dysphagia
NCT05190718 ·Status: RECRUITING