Skip to main content
Clinical Trials/NCT05126823
NCT05126823Active, not recruitingNot Applicable

Efficacy of a Combined Acceptance and Commitment Intervention to Improve Psychological Flexibility and Associated Symptoms in Cancer Patients: a Randomized Controlled Clinical Trial

Francisco Garcia Torres1 site in 1 country120 target enrollmentStarted: February 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
120
Locations
1
Primary Endpoint
Mean of Psychological flexibility scores

Study Overview

Brief Summary

Introduction: emotional and physical alterations frequently appear in cancer patients. In this sense, interventions based on acceptance and commitment therapy (ACT) show their efficacy to improve these symptoms through increased psychological flexibility, however, there is little evidence of the efficacy of ACT using combined modality (face-to-face + app), despite the fact that this application modality may have beneficial effects in this group of patients, who may see their participation in the interventions limited as a consequence of the disease.

Method / design: Cancer patients will be randomly assigned to one of the following groups: (1) face-to-face ACT + app group, (2) face-to-face ACT group, and (3) group receiving usual treatment. The planned interventions last between 8 and 10 weeks and include experiential exercises, metaphors, discussions, and homework assignments to promote awareness and flexibility about thoughts and emotions associated with cancer. In the group that uses the app, exercises (mindfulness, breathing), reminder systems, recording, reinforcement and monitoring will also be provided. It is estimated that a total of 112 participants (38 per group) will be necessary, and four evaluations will be carried out: T0 (pre-treatment), T1 (post-treatment, T2 (follow-up at three months) and T3 (follow-up at six months). months).

Hypothesis : The primary results that are expected to be obtained are a significant increase in the psychological flexibility of patients receiving treatment, with greater flexibility in the group receiving the combined intervention, evaluated with the AAQ-II. Furthermore, as secondary outcomes, it is expected to obtain significant improvements in anxiety and depression (HADS), quality of life (EORTC QLQ C-30), Fatigue (BFI), Insomnia (ISI) and post-traumatic growth (PTGI-SF).

Hypothesis: the efficacy of the ACT-based intervention in cancer patients may be increased if the benefits of using a modality that combines face-to-face and not face-to-face are added to it.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •The inclusion criteria for participants are:
  • •Men and women, aged between 18 and 70 years.
  • •Cancer diagnosis, stages I-III.
  • •Cancer type: Breast / Lung / Colorectal.
  • •Eligible for or currently receiving cancer treatment.
  • •Ability to be fluent in Spanish.
  • •Have a smartphone with daily access and basic smartphone / application management skills.
  • •Access to email account and internet.
  • •Not currently participating in another clinical trial.
  • •Not currently receiving other psychological treatment.

Exclusion Criteria

  • •for participants in the trial:
  • •Men and women aged> 70 years.
  • •Diagnosis of cancer, stage IV or other types of cancer.
  • •Not eligible for treatment.
  • •Inability to handle himself fluently in Spanish.
  • •Not having a smartphone with daily access and basic smartphone / application skills.
  • •Not having access to an email account and the internet.
  • •Currently participating in another clinical trial.
  • •Currently receiving other psychological treatment.

Arms & Interventions

ACT face-to-face + app

Experimental

Combines face-to-face ACT sessions with non-face-to-face activities and resources (mobile applications)

Intervention: Acceptance and commitment therapy + app (Behavioral)

ACT face-to-face

Active Comparator

face-to-face ACT sessions

Intervention: Acceptance and commitment therapy (Behavioral)

Waitlist

No Intervention

Waitlist group. After the second assessment of the two ACT groups (at post-treatment) this group will receive the face to face ACT intervention.

Outcomes

Primary Outcomes

Mean of Psychological flexibility scores

Time Frame: Change of mean scores of psychological flexibility from baseline to immediately after intervention

Acceptance and Action Questionnaire- II (AAQ-II). This instrument is designed to assess experiential avoidance and psychological inflexibility through 7 items that are answered with a Likert-type scale from 1 (never true) to 7 (always true) and a higher score indicates greater experiential avoidance (Bond et al., 2011).

Secondary Outcomes

  • Mean of Fatigue scores(Change of mean scores of fatigue from baseline to immediately after intervention)
  • Mean of Anxiety and Depression scores(Change of mean scores of anxiety and depression from baseline to immediately after intervention)
  • Mean of Quality of Life scores using EORTC QLQ C-30(Change of mean scores of the different subscales of quality of life from baseline to immediately after intervention)
  • Mean of Insomnia scores(Change of mean scores of insomnia from baseline to immediately after intervention)
  • Mean in Post-Traumatic growth scores(Change of mean scores of post-traumatic growth from baseline to immediately after intervention)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Francisco Garcia Torres

Lecturer

Universidad de Córdoba

Study Sites (1)

Loading locations...

Similar Trials

Efficacy of a Combined ACT+ App... | Clinical Trial