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Remote Assessment of Pain and Recovery Quality After Surgery Using a Digital Form: A Pilot Study

26. august 2026 oppdatert av: Fabricio Tavares Mendonca, Hospital de Base

After surgery, doctors need to know how patients are doing, especially in the first hours after they leave the recovery room. This can be hard to track once patients go to a regular hospital room, and some symptoms - like pain or nausea - may go unnoticed.

This study tests whether an online form, sent to patients' phones, can help doctors check on pain and recovery in the first 12 and 24 hours after surgery. Patients (or a family member helping them) will receive a link by WhatsApp and answer a short set of questions about their pain, nausea, medications, and how they are recovering.

The main goal is to find out whether patients are willing and able to use this online form, and whether it is a helpful and practical way to follow up with them after surgery.

Studieoversikt

Detaljert beskrivelse

Postoperative recovery is a dynamic process requiring continuous monitoring. After discharge from the post-anesthesia care unit (PACU), patients are typically assessed only through periodic in-person visits by the ward staff, which can create gaps in surveillance and lead to underreporting of pain, nausea, and other symptoms during the immediate postoperative period. Digital tools have been proposed as a way to narrow this gap by allowing patients to report symptoms directly and continuously, potentially enabling earlier identification of complications and more timely clinical response.

Despite promising results from international studies on postoperative digital monitoring, reviews have identified important gaps, including methodological heterogeneity, a lack of standardized and validated instruments, and limited integration with clinical teams. There is a particular scarcity of studies evaluating simple, accessible digital tools for the immediate postoperative period in Brazilian public hospitals.

This pilot study was designed to address that gap by testing a simplified, purpose-built digital form for remote postoperative follow-up. During the pre-anesthetic evaluation, patients (or an accompanying caregiver, when needed) are given a link, sent via WhatsApp, to a web-responsive online questionnaire designed for ease of use among postoperative patients. The form includes 18 questions covering pain at rest and during movement, nausea and vomiting, use of rescue analgesics and antiemetics, need for anesthesiology team intervention, functional recovery (ability to urinate and defecate), and overall satisfaction with the recovery process and with the questionnaire itself. Patients are asked to complete the form at two time points: 12 and 24 hours after PACU discharge.

The study's central hypothesis is that a simplified digital form is a feasible and well-accepted tool for remote postoperative monitoring, and that it can capture clinically meaningful data on pain, adverse effects, and perceived recovery. Findings from this pilot are intended to inform the future development of digital follow-up protocols - including potential integration with electronic medical records - for postoperative care in Brazilian public hospital settings, and to identify barriers to more equitable implementation of remote monitoring tools.

Studietype

Observasjonsmessig

Registrering (Antatt)

213

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Federal District
      • Brasília, Federal District, Brasil, 70.335-902
        • Hospital de Base do Distrito Federal (Instituto de Gestão Estratégica de Saúde do Distrito Federal - IGESDF)
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

Adult patients undergoing elective surgery not intended for postoperative intensive care unit (ICU) admission, consecutively enrolled at a single tertiary public hospital in the Federal District, Brazil. Patients are approached during the pre-anesthetic evaluation and, if eligible and willing to participate, are followed remotely via a digital form during the first 24 hours after discharge from the post-anesthesia care unit (PACU).

Beskrivelse

Inclusion Criteria:

  • Age ≥ 18 years
  • Undergoing elective surgery with anticipated discharge from the post-anesthesia care unit (PACU) to the ward
  • Access to a smartphone with internet connection (personally, or through an accompanying caregiver)
  • Cognitive capacity to respond to the digital form, or availability of a caregiver to respond on the patient's behalf
  • Signed Informed Consent Form

Exclusion Criteria:

  • Anticipated postoperative admission to the intensive care unit (ICU)
  • Inability to communicate, with no caregiver available to assist
  • Refusal to participate or to use the digital tool
  • No access to a mobile device/internet during the first 24 postoperative hours, with no logistical alternative available
  • Clinical condition that, at the discretion of the assisting team, contraindicates participation

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
Postoperative Patients (Digital Form Cohort)
Adult patients (≥18 years) undergoing elective, non-ICU-bound surgery at a tertiary public hospital, who completed a digital web-based form to report pain, nausea/vomiting, medication use, functional recovery, and satisfaction at 12 and 24 hours after PACU discharge.
A responsive, 18-item online questionnaire, accessed via a WhatsApp link, used to remotely collect patient-reported data on pain, nausea/vomiting, medication use, functional recovery, and satisfaction at 12 and 24 hours after PACU discharge. This is a data-collection tool and does not constitute a clinical/therapeutic intervention.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Adherence Rate to the Digital Follow-up Form
Tidsramme: At 12 hours and at 24 hours after PACU discharge
Proportion of enrolled patients who fully completed the digital questionnaire, calculated separately at 12 and 24 hours after discharge from the post-anesthesia care unit (PACU).
At 12 hours and at 24 hours after PACU discharge

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. oktober 2026

Primær fullføring (Antatt)

30. september 2027

Studiet fullført (Antatt)

30. september 2027

Datoer for studieregistrering

Først innsendt

26. august 2026

Først innsendt som oppfylte QC-kriteriene

26. august 2026

Først lagt ut (Faktiske)

31. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

31. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

26. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

UBESLUTTE

IPD-planbeskrivelse

A decision regarding individual participant data sharing has not yet been made. Data are currently stored on a secure digital platform with restricted access limited to the research team, in accordance with the approved research protocol. Any future data-sharing plan will comply with applicable Brazilian data protection and research ethics regulations (Law No. 14,874/2024; CNS Resolution No. 466/2012) and will be submitted for review by the Research Ethics Committee (CEP/IGESDF) before implementation.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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