Integrative Oncology for Patient Symptoms

Sponsor
Shaare Zedek Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT04940780
Collaborator
(none)
750
1
2
38
19.7

Study Details

Study Description

Brief Summary

The use of complementary and integrative medicine (CIM) among oncology patients is widespread, with a large body of research-based evidence supporting the ability of these therapies to alleviate symptoms related to cancer and its treatment. Organizations such as the American Society for Clinical Oncology and the European Society for Medical Oncology have included CIM modalities in their treatment guidelines, and many of today's leading cancer centers include CIM in their supportive care service. The proposed study will prospectively examine the impact of a CIM treatment program on the symptom burden, quality of life and function of patients undergoing active oncology treatment.

A total of 750 patients will undergo an integrative oncologist (IP) consultation followed by a series of 8 CIM treatments consisting of either acupuncture or touch-related therapies (reflexology, Shiatsu, Tuina, etc.) with the goal of relieving their symptoms. Patients will be allocated to one of the two study treatment arms: the "Patient-Preference Arm", for patients who specify their preference for either acupuncture or touch therapy; and the "Randomized Treatment Arm", for those with no preference, to be randomly allocated to either the acupuncture or touch-therapy subgroup. Patients will be asked to complete the following study questionnaires before and after the treatment regimen: the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30); the Edmonton Symptom Assessment System (ESAS); and the Measure Yourself Concerns and Wellbeing (MYCAW) tool. The primary study outcome will be the change in EORTC Global Health-Status / Quality of Life scores, from pre- to post-treatment. Secondary study outcomes will include EORTC QLQ-C30 functional and symptom scales, single items assessing additional symptoms commonly reported by cancer patients, and perceived financial impact of the disease; ESAS severity scores for 10 quality-of life related items; and MYCAW severity scores for the 2 most significant symptoms, as well as post-treatment narratives. Other secondary outcomes to be assessed include the safety of the study treatments (adverse effects); adherence to conventional treatment regimen; and narratives from the patient's informal caregiver (spouse, parent/child, sibling, friend, etc.).

Condition or Disease Intervention/Treatment Phase
  • Other: Acupuncture
  • Other: Touch Therapies
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
750 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Patient-preference, pragmatic methodologyPatient-preference, pragmatic methodology
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Examining the Impact of an Integrative Oncology Program on Patient Symptoms and Quality of Life: a Prospective Pragmatic Registry Protocol Study
Actual Study Start Date :
Nov 1, 2021
Anticipated Primary Completion Date :
Jul 31, 2024
Anticipated Study Completion Date :
Jan 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Patient Preference Arm

patients who specify their preference for either acupuncture or touch therapy

Other: Acupuncture
Acupuncture points will be selected on an individualized and symptom-directed basis, with the incorporation of points shown in clinical research to be effective for specific symptoms

Other: Touch Therapies
Touch therapies are to include Reflexology, Shiatsu and Therapeutic Touch

Active Comparator: Randomized Treatment Arm

with no preference, to be randomly allocated to either the acupuncture or touch-therapy subgroup

Other: Acupuncture
Acupuncture points will be selected on an individualized and symptom-directed basis, with the incorporation of points shown in clinical research to be effective for specific symptoms

Other: Touch Therapies
Touch therapies are to include Reflexology, Shiatsu and Therapeutic Touch

Outcome Measures

Primary Outcome Measures

  1. EORTC QLQ-C30 global health status / QoL scale [8 weeks]

    Change from baseline to the end of the 8-week integrative treatment program

Secondary Outcome Measures

  1. EORTC QLQ-C30 global health status / QoL scale [16 weeks]

    Change from baseline and 8-week assessment to 16 week follow-up

  2. EORTC QLQ-C30 - additional outcomes [From baseline to 8- (end of treatment program) and 16-week (post-program) assessment]

    Change in functional and symptom scores

  3. ESAS symptom severity scores [From baseline to 8- (end of treatment program) and 16-week (post-program) assessment]

    Change in severity scores for 10 quality-of life related items

  4. MYCAW symptom severity scores [From baseline to 8- (end of treatment program) and 16-week (post-program) assessment]

    Change in severity scores for the 2 most significant symptoms, as well as post-treatment narratives

  5. Frequency of adverse effects [At the end of the series of 8 weekly CIM treatment sessions (≤ 2 weeks after the last treatment session); after 16 weeks from baseline.]

    Any reported adverse events taking place during the study period which are considered to have possibly/probably resulted from the CIM intervention

  6. Adherence to conventional oncology treatment regimen [At 16 weeks from baseline.]

    Adherence to oncology treatment to be measured using the Relative Dose Intensity (RDI) calculation

  7. Caregiver expectations [At baseline]

    Narratives from the patient's informal caregiver (spouse, parent/child, sibling, friend, etc.).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • age ≥ 18 years

  • undergoing active oncology treatment

  • fully understand the study plan

  • agree to sign the study informed consent form.

Exclusion Criteria:
  • not fulfilling all of the study criteria

  • not interested in attending all 8 weekly CIM treatments sessions

Contacts and Locations

Locations

Site City State Country Postal Code
1 Institute of Oncology, Shaare Zedek Medical Center Jerusalem Israel 7791031

Sponsors and Collaborators

  • Shaare Zedek Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Noah Samuels, Director, Center for Integrative Complementary Medicine, Shaare Zedek Medical Center
ClinicalTrials.gov Identifier:
NCT04940780
Other Study ID Numbers:
  • INTEGR.ONCOL.REGIST-2021
First Posted:
Jun 28, 2021
Last Update Posted:
Apr 15, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Noah Samuels, Director, Center for Integrative Complementary Medicine, Shaare Zedek Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 15, 2022