Clinical trial · Interventional
Telehealth for the Self-Management of Dietary Quality of Life in Patients After Stomach Cancer Surgery
Telehealth Intervention for Self-Management of Dietary Quality of Life After Gastric Cancer Surgery
NCT05203627CI-TRIAL-00122838active not recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This clinical trial test whether taking part in a diet support intervention will help with patients nutrition and quality of life after surgery for esophagus or stomach cancer. The information learned by doing this research study may help patients get more information and/or support on eating after esophagus and stomach cancer surgery.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Gastric Carcinoma | Gastric Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Gastroesophageal Junction Adenocarcinoma | Gastroesophageal Junction Adenocarcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Best Practice | Other | — | UNRESOLVED |
| Questionnaire Administration | Other | — | UNRESOLVED |
| Telemedicine Visit | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Arm I (telehealth session, guidebook)
- description
- Patients receive 4 telehealth sessions over 1 hour each over 4 months. Patients also receive an intervention guidebook.
- interventionNames
- Other: Questionnaire Administration
- Other: Telemedicine Visit
- type
- ACTIVE_COMPARATOR
- label
- Arm II (standard nutritional support)
- description
- Patients receive standard nutritional support.
- interventionNames
- Other: Best Practice
- Other: Questionnaire Administration
Primary outcomes (13)
- measure
- Feasibility of the Telehealth Intervention - Percent Participation
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 21 Years
Show eligibility criteria text
Inclusion Criteria: * The ability to understand English or Spanish. * Undergone curative intent surgery for gastric or gastroesophageal (GE) junction cancer. * Began oral intake within the past month. * Aged 21 years and older. * Able to participate in telehealth sessions. * This study will be conducted in patients aged 21 years or older who have undergone curative intent surgery for gastric or GE junction cancer. * Age criterion for this trial is based on the National Institute of Health (NIH')s age criteria, which defines an adult as individuals aged 21 years and over. There are no restrictions related to performance status or life expectancy. * All subjects must have the ability to understand and the willingness to sign a written informed consent. Exclusion Criteria: * Subjects, who in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study.
References
Publications (0)
Data not yet available
No reference posted for this study.