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Completed

NCT Number: NCT03557762

The SEAMLESS Study: Smartphone App-based Mindfulness for Cancer Survivors

Smartphone app-based health interventions are an innovative way to deliver psychosocial cancer-care. In the SEAMLESS study, the investigators aim to evaluate a 4 week smartphone app-based mind-body intervention (MBI) in cancer survivors post-treatment. This is a randomized controlled trial, with a waitlist control group. Participants will be assigned to either receive the intervention immediately after enrollment or will need to wait for 3 months to receive the intervention.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Psychosocial Oncology, Cancer Control Alberta

Calgary, Alberta, T2N 3C1, Canada

About this study

BACKGROUND Cancer patients who are in the transition phase to survivorship after completing their final treatments need psychosocial interventions to manage stressors such as anxiety, depression, and fear of cancer recurrence. Smartphone app-based health interventions are an innovative way to deliver psychosocial cancer-care. In the SEAMLESS study, the investigators aim to evaluate an app-based mind-body intervention (MBI) in cancer survivors.

The need for psychosocial interventions for cancer survivors has been highlighted by the Institute of Medicine in their landmark survivorship report appropriately titled, "Lost in Transition." Cancer survivors are often unable to participate in face-to-face interventions because of difficulties such as compromised immunity, treatment-related side-effects, scheduling conflicts and geography. A smartphone-app based MBI can overcome several such difficulties, since patients can participate at their own convenience without the burden of travel and scheduling classes.

INTERVENTION DESIGN The AM smartphone app supports personalized mindfulness practices through lessons and personalized guided-meditation playlists; AM reportedly reduced anxiety in a study with college students. AM interprets its users' emotional state, e.g. angry, elated, from a user-inputted digital emotion-mapping board; and heart-rate data through algorithms that analyze facial bio-signals. The SEAMLESS study is a randomized wait-list controlled trial, which will evaluate AM's effectiveness for reducing stress (primary outcome), anxiety, depression, fatigue and fear of cancer recurrence in cancer survivors who have completed all treatments for 2 weeks or more. Outcomes will be assessed online using validated PROMIS measures at 1) baseline, 2) mid-point 3) immediately post-intervention, 4&5) 3 and 6 months follow-up post-baseline.

SIGNIFICANCE Cancer-care providers are uncertain about the efficacy of app-based interventions for patients, which are available in great supply in today's digital world. This study will provide rigorously evaluated efficacy data for an app-based MBI for cancer survivors, which if helpful, could be made easily available for psychosocial care at cancer centers worldwide.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women over the age of 18
  • Diagnosed with any type of cancer (stage I-III)
  • Completed active treatment (i.e. surgery, chemotherapy, radiation therapy) at least 4 months previously (ongoing hormonal therapies, AIs, tamoxifen, herceptin are not exclusionary)
  • Have access to a smartphone with data connection; in case patients' do not have a data plan or an insufficient data plan with their smart phone, we will pay for their data connection (up to 0.5GB/month)
  • Willing to devote 20-30 mins of time to do the mindfulness meditations and practices every day
  • Sufficient cognitive function to participate in the smartphone app-based intervention
  • Ability to speak and write English sufficiently to complete questionnaires

Exclusion criteria

  • Metastatic patients and those with ongoing chemotherapy (metastatic patients may not be stable enough to participate in the interventions and follow-up assessments).
  • Cognitive impairment that would interfere with completing questionnaires or the intervention.
  • Suffering from current Major Depressive Disorder, Bipolar Disorder or other psychiatric disorder that would interfere with the ability to participate.
  • Practicing smartphone app-based mindfulness more than or equal to once a week

Treatment and study plan

Mindfulness

Behavioral

A psychological behavioral intervention that trains participants in mindfulness techniques, which involves achieving a moment-to-moment non-judgmental awareness of their internal psychosocial-emotional state, through meditation and gentle mindful movements.

Primary outcomes

  1. Symptoms of Stress

    Time frame: 3 months

    Calgary - Symptoms of Stress Inventory (C-SOSI)

Secondary outcomes

  1. Fear of Cancer Recurrence

    Time frame: 3 months

    Fear of Cancer Recurrence Inventory (FCRI)

  2. Anxiety - PROMIS

    Time frame: 3 months

    PROMIS- Cancer Bank v1.0 - Anxiety

  3. Depression - PROMIS

    Time frame: 3 months

    PROMIS- Cancer Bank v1.0 - Depression

  4. Fatigue - PROMIS

    Time frame: 3 months

    PROMIS- Cancer Bank v1.0 - Fatigue

  5. Physical Function - PROMIS

    Time frame: 3 months

    PROMIS- Cancer Bank v1.1 - Physical Function

  6. App-based User Data

    Time frame: 3 months

    Users' self-reported stress, biometrics and engagement

Sponsors and collaborators

Lead sponsor

University of Calgary

Other

Registry information

Official study title

The SEAMLESS Study: A Clinical Trial Evaluation of a SmartphonE App-based MindfuLnEss Intervention for Cancer SurvivorS

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Jun 15, 2018
Registry last updated
May 23, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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