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High-intensity Interval Training Combined with Muscle-strength Training in Older Women

Feasibility and Preliminary Efficacy of High-intensity Interval Training Combined with Muscle-strength Training in Older Women: Pilot Randomized Controlled Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06825130
Enrollment
20
Registered
2025-02-13
Start date
2025-02-01
Completion date
2026-12-31
Last updated
2025-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Older Adult

Keywords

Women, HIIT, Resistance exercise, Combined exercise

Brief summary

Women generally live longer than men but often experience a faster muscle mass loss due to inactivity, which can lead to weakness and disability. Despite these risks, women, particularly older women, are less active than men. In England, less than one-third of women engage in sufficient aerobic activity, and less than 5% do enough muscle strength training. Common reasons for not exercising include lack of time and enjoyment. High-intensity interval training (HIIT) is an efficient and effective way to exercise that many women find more enjoyable than longer workouts. HIIT has been shown to be effective in older women, helping them improve their fitness with less time commitment. Because HIIT is time-efficient, it can be combined with muscle strength training without significantly increasing the duration of the exercise session, which may lead to even better fitness results. This study will assess how practical it is for older women to do HIIT and strength exercise combined training. It will also investigate whether this combined approach can improve overall fitness, muscle strength, aerobic fitness, and quality of life more than HIIT alone.

Interventions

BEHAVIORALExercise

Participants will attend 30-min training sessions 3 times a week for 12 weeks. The intensity of HIIT will be at 80% HR@VT2 measured in the first week and will increase to 90% in the second week. By week 3, the intensity will reach HR@VT2.

Sponsors

University of Nottingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Females (biologically at birth) * At least 60 years of age at the time of signing the informed consent * Non-smoker, including electronic cigarettes * Not participating in routine high-intensity aerobic or muscle strength exercise training (≥ 75 min/week of structured vigorous aerobic exercise, or 2 times /week of structured muscle strength training) * Able to perform a cardiopulmonary exercise testing (CPET) to exhaustion * willing to complete baseline and follow-up measures, and attend prescribed exercise sessions at the University of Nottingham * willing and able to give informed consent for participation in the study

Exclusion criteria

* Diagnosed with cardiovascular disease, kidney disease, diabetes, obstructive pulmonary disease, or uncontrolled hypertension * History or current neurological or psychiatric illness, or motor or cognitive restrictions * Contraindications to symptom-limited cardiopulmonary exercise testing (CPET), including resting hypertension with systolic blood pressure \>200 mmHg or diastolic blood pressure \> 110 mmHg, uncorrected medical conditions, such as significant anemia, important electrolyte imbalance, and hyperthyroidism, mental impairment with limited ability to cooperate, physical disability that precludes safe and adequate testing. * Having taken part in a research study in the last 3 months involving invasive procedures or an inconvenience allowance.

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of high-intensity interval training combined with muscle strength trainingFrom recruitment to week-12will be assessed from recruitment, adherence, compliance, safety, subjective exercise experiences and self-efficacy. Recruitment will be assessed by the proportion of patients remained interested and randomized after being informed of the requirements of the study; adherence will be assessed by the attendance to the prescribed exercise sessions; and compliance will be assessed by the proportion of participants adhering to prescribed exercise intensity. For safety, all mild, moderate, and severe symptoms and adverse events throughout this study will be recorded.

Secondary

MeasureTime frameDescription
functional capacityFrom baseline to week-12will be assessed using the Fullerton Functional Fitness Test, a valid and reliable measure of functional independence in older adults
muscle functionFrom baseline to week-12Isometric strength, isokinetic muscle torque (i.e., strength) and fatigue will be measured using a dynamometer (CYBEX).
cardiorespiratory fitnessFrom baseline to week-12will be measured by a gold-standard, symptom-limited CPET using metabolic equipment on an electronically braked cycle ergometer.
muscle massFrom baseline to week-12will be measured using ultrasound at the mind-point of the thigh, from the greater trochanter to mid patella.
QoLFrom baseline to week-12will be assessed using Short Form 36 Health Survey Questionnaire (SF-36).

Countries

United Kingdom

Contacts

Primary ContactTasuku Terada, PhD
tasuku.terada@nottingham.ac.uk441158230141

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026